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Blood Agar (BA)

30

Box/10 plates

- Thickness of agar plates: 3-7mm. - Color: true to the typical color of the environment. - Jelly surface: smooth, no foam, uniform, no layering, dry. - Sterility: no bacteria growth after incubation at 35 - 37oC/16-24 hours. - The packaging is intact, not cracked, broken, or torn. - The name of the goods must be clear and not confused with other goods. - Small packaging (5-10 discs/package or box). - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); or exchange for new goods when the Testing Department cannot use all the goods delivered to the Testing Department with a shelf life of <6 months. - The biological product quality inspection card must be dry and attached to the goods. - Goods are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Mac-Conkey Agar (MC)

30

Box/10 plates

- Thickness of agar plates: 3-7mm. - Color: true to the typical color of the environment. - Jelly surface: smooth, no foam, uniform, no layering, dry. - Sterility: no bacteria growth after incubation at 35 - 37oC/16-24 hours. - The packaging is intact, not cracked, broken, or torn. - The name of the goods must be clear and not confused with other goods. - Small packaging (5-10 discs/package or box). - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); or exchange for new goods when the Testing Department cannot use all the goods delivered to the Testing Department with a shelf life of <6 months. - The biological product quality inspection card must be dry and attached to the goods. - Goods are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Mannitol Salt Agar (MSA)

10

Box/10 plates

- Thickness of agar plates: 3-7mm. - Color: true to the typical color of the environment. - Jelly surface: smooth, no foam, uniform, no layering, dry. - Sterility: no bacteria growth after incubation at 35 - 37oC/16-24 hours. - The packaging is intact, not cracked, broken, or torn. - The name of the goods must be clear and not confused with other goods. - Small packaging (5-10 discs/package or box). - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); or exchange for new goods when the Testing Department cannot use all the goods delivered to the Testing Department with a shelf life of <6 months. - The biological product quality inspection card must be dry and attached to the goods. - Goods are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Sabouraub (SAB)

40

Box/10 plates

- Thickness of agar plates: 3-7mm. - Color: true to the typical color of the environment. - Jelly surface: smooth, no foam, uniform, no layering, dry. - Sterility: no bacteria growth after incubation at 35 - 37oC/16-24 hours. - The packaging is intact, not cracked, broken, or torn. - The name of the goods must be clear and not confused with other goods. - Small packaging (5-10 discs/package or box). - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); or exchange for new goods when the Testing Department cannot use all the goods delivered to the Testing Department with a shelf life of <6 months. - The biological product quality inspection card must be dry and attached to the goods. - Goods are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Salmonllea Shiegella Agar (SS)

20

Box/10 plates

- Thickness of agar plates: 3-7mm. - Color: true to the typical color of the environment. - Jelly surface: smooth, no foam, uniform, no layering, dry. - Sterility: no bacteria growth after incubation at 35 - 37oC/16-24 hours. - The packaging is intact, not cracked, broken, or torn. - The name of the goods must be clear and not confused with other goods. - Small packaging (5-10 discs/package or box). - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); or exchange for new goods when the Testing Department cannot use all the goods delivered to the Testing Department with a shelf life of <6 months. - The biological product quality inspection card must be dry and attached to the goods. - Goods are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Mueller - Hinton Agar (MHA)

20

Box/10 plates

- Thickness of agar plates: 3-7mm. - Color: true to the typical color of the environment. - Jelly surface: smooth, no foam, uniform, no layering, dry. - Sterility: no bacteria growth after incubation at 35 - 37oC/16-24 hours. - The packaging is intact, not cracked, broken, or torn. - The name of the goods must be clear and not confused with other goods. - Small packaging (5-10 discs/package or box). - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); or exchange for new goods when the Testing Department cannot use all the goods delivered to the Testing Department with a shelf life of <6 months. - The biological product quality inspection card must be dry and attached to the goods. - Goods are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Mueller- Hinton Blood Agar (MHBA)

2

Box/10 plates

- Thickness of agar plates: 3-7mm. - Color: true to the typical color of the environment. - Jelly surface: smooth, no foam, uniform, no layering, dry. - Sterility: no bacteria growth after incubation at 35 - 37oC/16-24 hours. - The packaging is intact, not cracked, broken, or torn. - The name of the goods must be clear and not confused with other goods. - Small packaging (5-10 discs/package or box). - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); or exchange for new goods when the Testing Department cannot use all the goods delivered to the Testing Department with a shelf life of <6 months. - The biological product quality inspection card must be dry and attached to the goods. - Goods are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

2-phase blood culture bottle (BHI)

100

Bottle

- The packaging is intact, not cracked, broken, or torn. - The container is easy to open, ensuring safety for users and quality of goods. - The name of the product must be clear and not confused with other products. - The shelf life must be ≥ 18 - 24 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); - Must have specific instructions for use. - There must be a chemical safety data sheet (MSDS) attached to the product. - Product quality inspection form must be dry and attached to the product. - Products are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Anaerobic blood culture bottle

50

Bottle

- The packaging is intact, not cracked, broken, or torn. - The container is easy to open, ensuring safety for users and quality of goods. - The name of the product must be clear and not confused with other products. - The shelf life must be ≥ 18 - 24 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); - Must have specific instructions for use. - There must be a chemical safety data sheet (MSDS) attached to the product. - Product quality inspection form must be dry and attached to the product. - Products are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

East dried rabbit plasma

6

Jar

- The packaging is intact, not cracked, broken, or torn. - The container is easy to open, ensuring safety for users and quality of goods. - The name of the product must be clear and not confused with other products. - The shelf life must be ≥ 18 - 24 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); - Must have specific instructions for use. - There must be a chemical safety data sheet (MSDS) attached to the product. - Product quality inspection form must be dry and attached to the product. - Products are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Normal Saline salt water

30

Vial/10ml

- The packaging is intact, not cracked, broken, or torn. - The container is easy to open, ensuring safety for users and quality of goods. - The name of the product must be clear and not confused with other products. - The shelf life must be ≥ 18 - 24 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); - Must have specific instructions for use. - There must be a chemical safety data sheet (MSDS) attached to the product. - Product quality inspection form must be dry and attached to the product. - Products are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

3% hydrogen peroxide

30

Vial (50mL)

- The packaging is intact, not cracked, broken, or torn. - The container is easy to open, ensuring safety for users and quality of goods. - The name of the product must be clear and not confused with other products. - The shelf life must be ≥ 18 - 24 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - Do not change batches within ≥ 6 months (each chemical must be used in the same batch for a stable period of ≥ 6 months); - Must have specific instructions for use. - There must be a chemical safety data sheet (MSDS) attached to the product. - Product quality inspection form must be dry and attached to the product. - Products are transported under the manufacturer's prescribed conditions.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Anti A

6

Vials (10ml)

- Available reagent set to determine the presence of antigen A on the surface of red blood cells based on the rules of antigen and antibody agglutination, by direct in vitro method. - Sensitivity, specificity, accuracy: 100%' - Chemicals are suitable for determining ABO blood group in humans - Instructions for use are included, Packaging is intact, not broken or torn, box must still be sealed intact, original label on vial must have full information (manufacturer, batch number, date of manufacture, expiry date, storage conditions) - Must have product quality certification; - Sensitivity: 100%, specificity 100%, agglutination reaction occurs within 5 - 10 seconds. - Expiry date must be guaranteed to be >12 months. - The name of the product must be clear and not confused with other products. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or information related to chemicals, it is necessary to immediately notify the Laboratory Department in writing.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Anti b

6

Vials (10ml)

- Available reagent set to determine the presence of B antigen on the surface of red blood cells based on the rules of antigen and antibody agglutination, by direct in vitro method. - Sensitivity, specificity, accuracy: 100%' - Chemicals are suitable for determining ABO blood group in humans - Instructions for use are included, Packaging is intact, not broken or torn, box must still be sealed intact, original label on vial must have full information (manufacturer, batch number, date of manufacture, expiry date, storage conditions) - Must have product quality certification; - Sensitivity: 100%, specificity 100%, agglutination reaction occurs within 5 - 10 seconds. - Expiry date must be guaranteed to be >12 months. - The name of the product must be clear and not confused with other products. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or information related to chemicals, it is necessary to immediately notify the Laboratory Department in writing.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Anti AB

6

Vials (10ml)

- Ready-made reagent set to determine the presence of A and B antigens on the surface of red blood cells based on the rules of antigen and antibody agglutination, by direct in vitro method. - Sensitivity, specificity, accuracy: 100%' - Chemicals are suitable for determining ABO blood group in humans - Instructions for use are included, Packaging is intact, not broken or torn, box must still be sealed intact, original label on vial must have full information (manufacturer, batch number, date of manufacture, expiry date, storage conditions) - Must have product quality certification; - Sensitivity: 100%, specificity 100%, agglutination reaction occurs within 5 - 10 seconds. - Expiry date must be guaranteed to be >12 months. - The name of the product must be clear and not confused with other products. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or information related to chemicals, it is necessary to immediately notify the Laboratory Department in writing.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Anti d igg/igm

6

Vials (10ml)

- Ready-made reagent set to determine the presence of D antigen on the surface of red blood cells based on the rules of antigen and antibody agglutination, by direct in vitro method. - Sensitivity, specificity, accuracy: 100%' - Chemicals are suitable for determining ABO blood group in humans - Instructions for use are included, Packaging is intact, not broken or torn, box must still be sealed intact, original label on vial must have full information (manufacturer, batch number, date of manufacture, expiry date, storage conditions) - Must have product quality certification; - Sensitivity: 100%, specificity 100%, agglutination reaction occurs within 5 - 10 seconds. - Expiry date must be guaranteed to be >12 months. - The name of the product must be clear and not confused with other products. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or information related to chemicals, it is necessary to immediately notify the Laboratory Department in writing.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Rapid Test HBsAb Cassette

50

kiểm TRA

- Cassette, immunochromatographic testing instrument based on the principle of one-dimensional chromatography - Detects HBeAb antibodies of hepatitis B virus in human serum or plasma samples. - Sensitivity: ≥ 96%. - Specificity: ≥ 99 % - Accuracy: ≥ 98 % - Stable at 2-30 °C ' - The product has clear and complete information on the label that can be distinguished from other products. - There is information about substances that interfere with the results. - There is information about cross-reactions affecting the results.N70 - The packaging is intact, not broken or torn, with seals. - The shelf life must be ≥ 12 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - Must have a certificate of goods quality. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or method of reading results, it is necessary to immediately notify the Laboratory Department in writing.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

HBeAg Rapid Test Cassette

50

kiểm TRA

- Test tray format (Cassette). Qualitative detection of HBeAg antigen in human serum and plasma samples. - Correlation sensitivity: ≥ 96%. - Correlation specificity ≥ 98%; - Anticoagulants such as heparin, EDTA and citrate do not affect test results - Hemolysis samples, blood fat samples, and jaundice do not affect test results. There is no cross-reactivity with samples containing rheumatoid factor, anti-HCV antibodies, anti-HIV antibodies and pregnant women. - The test kit is stable for at least 4 weeks when stored at a temperature of 55±1°C ' - The product has clear and complete information on the label that can be distinguished from other products. - There is information about substances that interfere with the results. - There is information about cross-reactions affecting the results.N70 - The packaging is intact, not broken or torn, with seals. - The shelf life must be ≥ 12 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - Must have a certificate of goods quality. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or method of reading results, it is necessary to immediately notify the Laboratory Department in writing

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Paraffin oil

1

Bottle (100mL)

- The product has clear and complete information on the label that can be distinguished from other products. - Small packaging (≤ 100mL). - Color: has the characteristic color of the reagent. - Homogeneous, no residue - Intact packaging, no cracks, breaks, or tears. - The container material does not interact with the dye ingredients. - The shelf life must be ≥ 12 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - There must be a certificate of goods quality according to the batch of goods. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or method of reading results, it is necessary to immediately notify the Laboratory Department in writing. ** Purity lens oil (d ≥ 1.030)

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Single dye (Methylene Blue)

1

Set (100mL)

- The product has clear and complete information on the label that can be distinguished from other products. - Small packaging (≤ 100mL). - Color: has the characteristic color of the reagent. - Homogeneous, no residue - Intact packaging, no cracks, breaks, or tears. - The container material does not interact with the dye ingredients. - The shelf life must be ≥ 12 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - There must be a certificate of goods quality according to the batch of goods. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or method of reading results, it is necessary to immediately notify the Laboratory Department in writing. ** Purity lens oil (d ≥ 1.030)

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Wright dyes

1

Set (100mL)

- The product has clear and complete information on the label that can be distinguished from other products. - Small packaging (≤ 100mL). - Color: has the characteristic color of the reagent. - Homogeneous, no residue - Intact packaging, no cracks, breaks, or tears. - The container material does not interact with the dye ingredients. - The shelf life must be ≥ 12 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - There must be a certificate of goods quality according to the batch of goods. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or method of reading results, it is necessary to immediately notify the Laboratory Department in writing. ** Purity lens oil (d ≥ 1.030)

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Widal kit

1

Kit/5ml

- Ready-to-use chemical kit for testing the detection of O and H antibodies of Salmanella, based on antigen- and antibody-specific agglutination reactions. - Includes negative and positive controls' - Products have clear and complete information on the label that can be distinguished from other products. - There is information about substances that interfere with the results. - There is information about cross-reactions affecting the results. - The packaging is intact, not broken or torn, and has a seal. - The shelf life must be ≥ 12 months compared to the maximum shelf life (calculated from the date of manufacture) of the product. - There must be a chemical safety data sheet (MSDS) attached to the product. - Must have specific instructions for use in Vietnamese or English. - Must have a certificate of goods quality. - Products are transported under the manufacturer's prescribed conditions. - When there is a change in specifications or method of reading results, it is necessary to immediately notify the Laboratory Department in writing.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

3% Lugol solution (500 ml)

5

Bottle/ 500ml

3% Iodine

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

3% Acetic Acid Solution (CH3COOH), 500 ml

5

Bottle/ 500ml

Acetic acid 3%

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Quantitative CA 125 test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Quantitative CA 15-3 test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Quantitative CA 19-9 test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

CEA quantification test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

AFP quantification test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Total PSA quantification test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Quantitative Free PSA test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Quantitative Toxoplasma IgM test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Quantitative Toxoplasma IgG test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Anti-HBs quantitative test

180

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Quantitative NT-proBNP test

300

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Rubella Virus IgG Quantification Test

300

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

Rubella Virus IgM Quantification Test

300

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City

I-hs Troponin I Quantification Test

3.000

kiểm TRA

- The kit includes pre-filled test tubes with the test name, manufacturer's name, lot number, expiration date, manufacturing date, storage conditions, etc., printed on the test tube. - The test format includes: 1 SPR (a single-use antibody-coated column tip, sealed with a label containing a barcode and information, and a chemical strip containing 10 wells for the necessary chemicals for a test, also sealed with a barcode label, the size of the chemical strip is 1.8cm x 15.3cm (width x length), each chemical strip is packaged individually as a ready-to-use test). - The kit must include standard and control samples with complete information. - If buffers are included, they must have clear and complete labeling as on the test tubes. - Information about interfering substances must be provided. - The test's detection and quantification thresholds must be specified. - The test method is fluorescent immunoassay (FEIA). - The following ranges and detection limits must be provided: + CA 125 ≤ 4 U/mL (Measurement range includes the range: 4-600 U/mL) + CA 15-3 ≤ 2 U/mL (Measurement range includes the range: 2-400 U/mL) + CA 19-9 ≤ 3 U/mL (Measurement range includes the range: 3-500 U/mL) + CEA ≤ 0.5 ng/mL (Measurement range includes the range: 0.5-200 ng/mL) + AFP ≤ 0.5 IU/mL (Measurement range includes the range: 0.5-400 IU/mL) + Total PSA ≤ 0.07 ng/mL (Measurement range includes the range: 0.7-100 ng/mL) + Free PSA ≤ 0.05 ng/mL (Measurement range includes the range: 0.05-10 ng/mL) + Toxoplasma IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Toxoplasma IgG measurement range includes the range: 0-300 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Anti-HBs ≤ 3 mIU/mL (Measurement range includes the range: 3-500 mIU/mL) + NT-ProBNP ≤ 15 pg/mL (Measurement range includes the range: 15-25.000 pg/mL) + Rubella IgG measurement range includes the range: 0-400 IU/mL, provides detailed results interpretation: Negative/Positive/Indeterminate based on measured values + Rubella IgM provides detailed results interpretation: Negative/Positive/Indeterminate based on Index value + Troponin I-hs (Measurement range includes the range: 1.5-40.000 ng/L) - The packaging must be intact, unopened, and undamaged, with a sealed label. - The product name must be clearly stated and not confused with other products. - The expiration date must be at least 6 months from the manufacturing date. - Lots cannot be exchanged within ≥ 3 months or new items cannot be swapped if the laboratory receiving them has an expiration date of < 3 months. - A Material Safety Data Sheet (MSDS) must be included with the product. - Specific instructions for use in Vietnamese or English must be provided. - A quality certificate for each shipment must be provided. - The products must be transported under the manufacturer's specified conditions. - Any changes to packaging, reading results, etc., must be immediately communicated to the laboratory in writing. - Compatible with MiniVidas/Vidas automated immunoassay systems. - The winning contractor is responsible for supplying medical equipment to use the test chemicals according to the owner's requirements. The contractor will not transfer ownership, but only transfer the right to operate and use the medical equipment to the hospital. Simultaneously, they commit to providing a solution for integrating the hospital's LIS, HIS, EMR software. - Ensure operational capacity and electrical safety during use (operation, maintenance, repair, and servicing) throughout the contract period.

63-65 Ben Van Don Street, Xom Chieu Ward, Ho Chi Minh City