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| No | List of product/services | Quantity | Unit | Description | Location | Specification | Note | Feature |
|---|---|---|---|---|---|---|---|---|
1 |
Chemical test CA125 |
25 |
Box |
- A luminescent microchemical microchemical test (CMIA) used to quantify antigen to determine OC 125 in serum and plasma.
- Ingredient :
+ Microparticle antibodies antigen CA125 (single -line antibody) covered with micro -seeds in tris cushions with protein stabilizers (from cows). Minimum concentration: about 0.09% solid. Preservatives: Sodium Azide and Prococ 300.
+ Conjugate combined with Ca125 antibodies (from single -line antibodies) marked with acidinium in phosphate buffer solution with protein stabilizer (from cow). Minimum concentration: about 0.075 μg/ml. Preservatives: Sodium Azide and Prococ 300.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
2 |
Chemical test shift 19-9 |
30 |
Box |
-Located microchemical microchemical test (CMIA) is used to quantify the reaction substance 1116-NS-19-9 in serum or human plasma. Used in combination with other clinical methods in supporting the treatment of pancreatic cancer patients.
- Ingredient:
+ Microparticle: 1116-NS-19-9 (single mouse, antibody) covered with micro-seeds in citrate buffer solution with protein stabilizer (cow). Minimum concentration: about 0.09% solid. Preservatives: Sodium Azide and Prococ 300.
+ Conjugate: 1116-NS-19-9 (single-line mice, single-line antibodies) combined with acidinium marks in phosphate buffer solution with protein stabilizer (cow). Minimum concentration: about 0.5 μg/ml. Spread: Sodium Azide and Proclin 300.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
3 |
Prolactin RGT test chemicals |
5 |
Box |
- Located microchemical microchemical test (CMIA) is used to quantify prolactin in serum and human plasma.
- Ingredient:
+ Microparticle: Anti-Prolactin (single-line antibodies, mice) covered with micro-seeds in a tris buffer solution with protein stabilizer (from cow and mouse). Minimum concentration: about 0.1% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: Anti-Prolactin combination substance (Mouse, single antibody) marked Acridinium in a phosphate buffer solution with protein stabilizer (from fish and cow). Minimum concentration: about 0.05 μg/ml. Preservatives: Procline.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
4 |
PSA Total chemicals |
30 |
Box |
-Located microchemical immune test (CMIA) to quantify total PSA (both free PSA and PSA complex with alpha-1-antichymotrypsin) in human serum
- Ingredient:
+ Microparticle: Anti-PSA (single-line antibodies) covered with micro-seeds in a tris buffer solution with protein stabilizer (from cow). Minimum concentration: about 0.1% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: A substance combined with anti-psa (single-line antibodies) marked with acidinium in mesic buffer solution with protein stabilizer (from cow). Minimum concentration: about 10 ng/ml. Preservatives: Anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
5 |
Chemical test Ca15-3 |
25 |
Box |
- Located microchemical immunosuppressive test (CMIA) used to quantify antigen DF3 in serum and plasma.
- Ingredient:
+ Microparticle: 115D8 (Mouse, single -line antibodies) covered with micro -seeds in the tris buffer solution with protein stabilizer (cow). Minimum concentration: about 0.09% solid. Preservatives: Sodium Azide and Proclin300.
+ Conjugate: DF3 ACIDIINUUM marker (Mouse, single -line antibody) in Phosphate buffer solution with stabilizerprotein (from cow). Minimum concentration: about 0.05 μg/ml. Preservatives: Sodium Azide and Prococ 300.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
6 |
Cyfra 21-1 test chemicals |
35 |
Box |
Is a microchemical immunosuppressant test (CMIA) used to quantify the 19 -pieces of cytokeratin in people in serum and plasma.
The measurement of the test is about 0.50 to 100.00 ng/ml (0.50 to 100.00 μg/l). Lob about 0.01 ng/ml (μg/l); LOD is about 0.05 ng/ml (μg/l); LOQ is about 0.15 ng/ml (μg/l).
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
7 |
NT-Probnp test chemicals |
190 |
Box |
Located microchemical immune test (CMIA) used to quantify Vitro Peptide Into Satri Type B with N -head amino acid at the end (ntprobnp) in serum and plasma.
The measurement concentration range from 8.3 to 35 000.0 PG/ml (1.0 to 4130.0 PMOL/L). Lob is about 5.8 g/ml; LOD is about 7.9 g/ml; Loq is about 8.3 g/ml
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
8 |
AFP testing chemicals |
43 |
Box |
- Micronutrated microchemical test (CMIA) to quantify alpha-fetoprotein (AFP)
- Ingredient:
+ Microparticle: Anti-AFP (single-line mouse, antibody) covered with micro-seeds in mesus cushions with protein stabilizers (from cows). Minimum level: about 0.1% solid. Preservatives: Proclin 300.
+ Conjugate: Anti-AFP (single-line antibodies, mice) combined with acidinium marks in mesic buffer solution with protein stabilizer (from cow). The minimum concentration of about 400 ng/ml. Preservatives: Sodium Azide and anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
9 |
CEA testing chemicals |
30 |
Box |
- Located microchemical microchemical test (CMIA) used to quantify antigen of embryo carcinoma (CEA) in serum and plasma samples
- Ingredient:
+ Microparticle: Anti-Jcea (single-line antibody, mouse) covered with micro-seeds in a tris buffer solution with protein stabilizer (from cow). Minimum concentration: about 0.1% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: A substance combined with CEA anti-antibody antibody marks ACIDIINUUM (Mouse, single-line antibody) Anti-Jcea in phosphate buffer solution with protein stabilizer (from cow). Minimum concentration: about 0.8 μg/ml. Preservatives: Anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
10 |
Cortisol testing chemicals |
120 |
Box |
- Located microchemical microchemical test (CMIA) used to quantify cortisol in serum or serum, plasma, or urine.
- Ingredient:
+ Microparticles: Anti-cortisol (single antibody, mouse) covered with microscopic micro-buffer solution Tris/bis-tris with protein stabilizer (from cow). Minimum concentration: about 0.09% solid. Preservatives: Proclin 300, Sodium Azide.
+ Conjugate: Cortisol combined with acidinium marks in citrate buffer solution with stabilizer with surfactant activity. The minimum concentration of about 0.7 ng/ml. Preservatives: Proclin 300.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
11 |
Ferritin testing chemicals |
25 |
Box |
- Located microchemical microchemical test (CMIA) used to quantify ferritin in serum and plasma
- Ingredient:
+ Microparticles: Anti-Ferritin (single-line rats, antibodies) on micro-seeds in a tris buffer solution with protein stabilizer (cow and mouse). Minimum concentration: about 0.125% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: A substance combined with anti-ferritin (rabbits, single-line antibodies) marked with acidinium in mes buffer solution with protein stabilizer (from cow). The minimum concentration of about 75 ng/ml. Preservatives: Anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
12 |
Free T3 testing chemicals |
30 |
Box |
- Located microchemical immunosuppressant (CMIA) used to quantify free triiodothyronine (free T3) in serum and plasma
- Specification: box 1200 test
- Ingredient:
+ Microparticles: Anti-T3 (from sheep) covered with seeds in a mes buffer solution with stabilizer from sheep IgG. The minimum concentration of 0.085% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: T3 combined with acidinium marks in citrate buffer solution with NaCl and Triton X-100 stabilizer. Minimum concentration: about 0.33 ng/ml. Preservatives: Anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box of 2 x 600 test |
||
13 |
Free T3 testing chemicals |
50 |
Box |
- Located microchemical immunosuppressant (CMIA) used to quantify free triiodothyronine (free T3) in serum and plasma
- Specification: 200 test box
- Ingredient:
+ Microparticles: Anti-T3 (from sheep) covered with seeds in a mes buffer solution with stabilizer from sheep IgG. The minimum concentration of 0.085% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: T3 combined with acidinium marks in citrate buffer solution with NaCl and Triton X-100 stabilizer. The minimum concentration of about 0.33 ng/ml. Preservatives: Anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
14 |
Free T4 testing chemicals |
32 |
Box |
- Located microchemical microchemical test (CMIA) is used to quantify free thyroxine (free T4) in serum and human plasma
- Specification: box 1200 test
- Ingredient:
+ Microparticles: Anti-T4 (from sheep) covered with micro-seeds in a tris buffer solution with stabilizer from sheep IgG. Minimum concentration of 0.05% solid. Preservatives: Sodium Azide.
+ Conjugate: A substance combined T3 marks ACridinium in mesic buffer solution with NaCl and Triton X-100 stabilizer. The minimum concentration is about 0.2 ng/ml. Preservatives: Procline.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box of 2 x 600 test |
||
15 |
Free T4 testing chemicals |
50 |
Box |
- Is a microchemical microchemical test (CMIA) used to quantify thyroxine free (free T4) in serum and human plasma
- Specification: 200 test box
- Ingredient:
+ Microparticles: Anti-T4 (from sheep) covered with micro-seeds in a tris buffer solution with stabilizer from sheep IgG. Minimum concentration of 0.05% solid. Preservatives: Sodium Azide.
+ Conjugate: A substance combined T3 marks ACridinium in mesic buffer solution with NaCl and Triton X-100 stabilizer. The minimum concentration is about 0.2 ng/ml. Preservatives: Procline.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
16 |
TSH testing chemicals |
36 |
Box |
- Located microchemical immunosuppressant test (CMIA) used to quantify the stimulating hormone (TSH) in serum and plasma samples
- Specification: box 1200 test.
- Ingredient:
+ Microparticles: Anti-β TSH (rat, single-line antibody) covered with micro-seeds in a tris buffer solution with protein stabilizer (from cow). Minimum concentration of 0.07% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: A substance combined with anti-α TSH (single mouse, single antibody) marks ACridinium in the mes buffer solution with protein stabilizer (from cow). The minimum concentration of about 60 ng/ml. Preservatives: Anti -microorganism agent.
+ Assay Diluent: Tris cushion. Preservatives: Anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box of 2 x 600 test |
||
17 |
TSH testing chemicals |
50 |
Box |
- Located microchemical immunosuppressant test (CMIA) used to quantify thyroid stimulating hormones (TSH) in serum and plasma samples
- Specification: 200 test box.
- Ingredient:
+ Microparticles: Anti-β TSH (rat, single-line antibody) covered with micro-seeds in a tris buffer solution with protein stabilizer (from cow). Minimum concentration of 0.07% solid. Preservatives: Anti -microorganism agent.
+ Conjugate: A substance combined with anti-α TSH (single mouse, single antibody) marks ACridinium in the mes buffer solution with protein stabilizer (from cow). The minimum concentration of about 60 ng/ml. Preservatives: Anti -microorganism agent.
+ Assay Diluent: Tris cushion. Preservatives: Anti -microorganism agent.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
18 |
B-R-A-H-M PCT test |
70 |
Box |
- Located microchemical microchemical test (CMIA) is used to quantify processonin (PCT) in serum and plasma.
- Ingredient:
+ Microparticles: Anti-PCT (single-line antibodies) covered with micro-seeds in tris cushions with protein stabilizers (from cows), mouse IgG, and triton X-405. The minimum concentration of 0.06% of the solid. Preservatives: Proclin 950 and sodium Azide.
+ Conjugate: Anti-PCT combined with acidinium marks (rats, single-line antibodies) in phosphate buffer solution with protein stabilizer (from cow) and triton x-405. The minimum concentration of about 270 ng/ml. Preservatives: Proclin 950 and sodium Azide. Proclin 300.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 2 x 100 test |
||
19 |
Chemicals Cell-All Reticulocyte |
6 |
Box |
- Perform analysis of red blood cells using total blood samples.
- Ingredient:
+ New methylene green ≤ 0.2 %
+ Potassium oxalate, monohydrate ≤ 3.0 %
+ Sodium phosphate, dibasic ≤ 0.3 %
+ Potassium phosphate, monobasic ≤ 0.05%
+ Disodium EDTA, Dihydrate ≤0.03%
+ Sodium chloride ≤ 1.0%
+ Surface ≤ 0.001%
+ Preservatives ≤ 0.05 %
(or equivalent) |
S.I.S International General Hospital Can Tho |
100 x 3.7 mL |
||
20 |
Hemoglobin measurement reagent |
15 |
Box |
- Chemicals used on hematological analysts have the function of rapid red blood cells, minimize the formation of cell pieces and keep the cell nucleus intact
- Ingredients: Quatnary ammonium salt ≤10%; Hydroxylamine salt ≤3%
(or equivalent) |
S.I.S International General Hospital Can Tho |
3.8 l |
||
21 |
Dilute solution and count platelet red blood cells |
35 |
Box |
- Chemicals used on hematological analysts with the function of stabilizing the volume of each red blood cell and platelet in the counting and division process, is an external solution for hydroelectricity, is a washing solution for the solution system.
- Ingredients include: sodium phosphate, dibasic ≤0.3%, potassium phosphate, monobasic ≤0.05%, Disodium edta, dihydrate ≤0.03%, sodium chloride ≤1.0%, Potassium chloride ≤0.05%, surface ≤0,002%, preservative ≤04%
(or equivalent) |
S.I.S International General Hospital Can Tho |
20 l |
||
22 |
White cell counting reagents |
30 |
Box |
- Chemicals used on hematological analysts with dilution function for leukocytes, separation by osmotic osmosis pressure, retaining the proper scattering properties of leukocytes, creating enough wet effects to prevent air bubbles, washing substances for white blood cell mixing chamber, dilution of red blood cells.
- Ingredients: Buffer ≤1.00%; Aromatic Oxy-alcohol ≤1.00%; Polyoxyethylene ether ≤0.10%
(or equivalent) |
S.I.S International General Hospital Can Tho |
3.8 l |
||
23 |
DIRECT LDL testing chemicals |
100 |
Box |
Is a test to quantify low density lipoprotein cholesterol (LDL) in serum or human plasma.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box of 2 x 290 test |
||
24 |
Ultra HDL testing chemicals |
35 |
Box |
Is a test to quantify high density lipoprotein cholesterol in serum or plasma.
- Method: Accelerator Selective Detergent
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 4 x 350 test |
||
25 |
Glucose testing chemicals |
20 |
Box |
- Used to quantify glucose concentration in plasma, serum, urine or cerebrospinal fluid (CSF) in humans.
- Measurement of serum/plasma glucose is about 5 to 800 mg/dl (0.28 to 44.40 mmol/l).
- The measurement concentration of the glucose test uses urine/CSF about 1 to 800 mg/dl (0.06 to 44.40 mmol/l).
-Method: Hexokinase/G-6-PDH
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 10 x 400 test |
||
26 |
Urea nitrogen testing chemicals |
19 |
Box |
Used to quantify urea nitrogen in serum, plasma or urine.
- Method: urease.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 10 x 400 test |
||
27 |
Creatinine testing chemicals |
20 |
Box |
Used for the quantitative determination of creatinine in human serum, plasma or urine.
Method: Kinetic Alkaline Picrate.
(or equivalent) |
S.I.S International General Hospital Can Tho |
10 x 450 test |
||
28 |
Uric acid tests |
40 |
Box |
To quantify uric acid in serum, plasma or urine.
- Method: enzyme uricase.
(or equivalent) |
S.I.S International General Hospital Can Tho |
4 x 160 Test |
||
29 |
Alanine Aminotransferase test chemicals |
65 |
Box |
To quantify alanine aminotransferase in serum and plasma.
This test is linearly in analytical measurement range of 7 to 3258 U/L (0.12 to 54.31 μkat/l).
(or equivalent) |
S.I.S International General Hospital Can Tho |
4 x 300 Tests |
||
30 |
Gamma- Glutamyl Transferase test chemicals |
90 |
Box |
To quantify gamma-glutamyl transferase in serum or plasma.
-Method: L-Gamma-Glutamyl-3-Carboxy-4-Nitroanilide.
(or equivalent) |
S.I.S International General Hospital Can Tho |
4 x 150 test |
||
31 |
Aspartate aminotransferase chemicals |
65 |
Box |
For the determination of aspartate aminotransferase in serum or plasma.
The analytical measurement range is from 5 to 4001 U/L (0.08 to 66.70 µkat/L). LoB 2 U/L, LoD 4 U/L, LoQ 5 U/L
(or equivalent) |
S.I.S International General Hospital Can Tho |
4 x 300 Tests |
||
32 |
Triglyceride testing chemicals |
45 |
Box |
To quantify triglycerides in serum or plasma.
- Method: Glycerol phosphate oxidase
(or equivalent) |
S.I.S International General Hospital Can Tho |
4 x 350 test |
||
33 |
Cholesterol testing chemicals |
16 |
Box |
To quantify cholesterol in serum or plasma.
(or equivalent) |
S.I.S International General Hospital Can Tho |
4x800 Test |
||
34 |
Chemical test Calcium2 |
12 |
Box |
Used to quantify calcium in serum, plasma or urine on the analytical machine.
- Method: Arsenazo III
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box 4 x 390 test |
||
35 |
Free T3 quantitative testing reagent |
390 |
Box |
- Serum and plasma testing reagents on automatic immune testing machines;
- Method: Enzyme immunity is competitive; Measurement range: approximately 0.88–30 PG/ml [1,4–46 pmol/l];
- Main ingredients: Thuan particles from streptavvidin in the buffer solution with protein (bird), surfactant substance, nan3, procline, mesic buffer solution, similar substance T3 biotin, protein (goat, cow, bird), combination of single-phosphate antibodies in alkaline in aces solution
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2x50test |
||
36 |
Free T4 quantitative test reagent |
390 |
Box |
Free T4 quantitative testing reagent in serum and human plasma (heparin) on automatic immune testing machines.
Method: 2 -step enzyme immunity; Measurement range: approximately 0.25-6.0 ng/dl [3,2-77.2 PMOL/l];
Main ingredients: Favorable particles from streptavvidin, tris cushion salt, surfactant substance, nan3, procline, alkaline phosphatase combination (cow) - triiodothyronin, antibody (single line, mouse) resistant thyroxin - T4 biotin, protein (bird and mouse)
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2x50test |
||
37 |
Albumin quantitative testing reagent |
10 |
Box |
Ingredients: Succinate buffer (pH 4.2) 100 mmol/L; Bromocresol green 0.2 mmol/L;
Method: Bromocresol Green; Linear range approximately 15 – 60 g/L (1.5 – 6.0 g/dL); Wavelength is about 600 nm; Sample type: Serum, plasma; Repeatability: CV ≤ 3%; Overall precision: CV ≤ 3%; Minimum number of tests/1 mL: 17 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x29ml |
||
38 |
Albumin quantitative testing reagent |
3 |
Box |
Ingredients: Succinate buffer (pH 4.2) 100 mmol/l; Bromocresol Green 0.2 mmol/l;
Method: Bromocresol Green; Linear range is about 15 - 60 g/l (1.5 - 6.0 g/dl); The wavelength is about 600 nm; Sample type: serum, plasma; Repeated level: CV ≤ 3%; Total bust: CV ≤ 3%; Minimum number of tests/1 ml: 16 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x54ml |
||
39 |
ALT quantitative test reagent |
65 |
Box |
- Ingredients: Tris buffer pH 7.15 (37 ° C) 100mmol/l; L-next 500mmol/l; 2-Oxoglutarate 12mmol/l; LDH 1.8ku/l; NADH 0.2mmol/l;
- Method: Based on IFCC's recommendations; Linear range is about 3 - 500 U/l (0.05 - 8.33 μkat/l); The wavelength is about 340 nm; Sample type: serum, plasma; Repeated level: CV ≤ 5%; Total bust: CV ≤ 10%; The minimum number of tests/1 ml: 6 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x50ml+4x25ml |
||
40 |
AST quantitative test reagent |
65 |
Box |
- Ingredients: Tris buffer, pH 7.65 (37 ° C) 80mmol/l; L-ASPARTATE 240mmol/l; 2-Oxoglutarate 12mmol/l; LDH ≥ 0.9ku/l; Mdh ≥ 0.6ku/l; NADH 0.2mmol/l;
- Method: Based on IFCC's recommendations; Linear range is about 3 - 1000 U/l (0.05 - 16.7 μkate/l); The wavelength is about 340 nm; Sample type: serum, plasma; Repeated level: CV ≤ 5%; Total bust: CV ≤ 10%; The minimum number of tests/1 ml: 10 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x25ml+4x25ml |
||
41 |
TSH quantitative testing reagent |
220 |
Box |
- Testing reagent in plasma or human serum on automatic immune testing machines;
- Method: immunity enzyme 2 location mounted "sandwich"; Measurement range: approximately 0.005 - 50.0 μiu/ml [miu/l];
- Main ingredients: The agreed particles from antibodies (rats, single -line) resistance to TSH people, Tris cushion salt, Surfactive substance, Beef serum albumin (BSA), Sodium Azide, Procline, antibody (mouse, single -line) TSH plus with alkali phosphate, Aces cushion, protein (mouse)
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2x100test |
||
42 |
Testing test reagent (calcium) |
10 |
Box |
- Ingredients: Imidazol (pH 6.9); Arsenazo III 0.02%;
- Method: Arsenazo III; Linear range: Serum, plasma about 1 - 5 mmol/l (4 - 20 mg/dl); Urine is about 0.1 - 10 mmol/l (0.4 - 40 mg/dl); Wavelength: about 660 nm; Sample type: serum, plasma, urine; Repeatedness ≤3% /total bust: ≤ 4%; Minimum number of tests/1 ml: 33 Test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x15ml |
||
43 |
Cholesterol quantitative testing reagent |
10 |
Box |
- Ingredients: Phosphate buffer solution (pH 6.5) 103 mmol/l; 4-aminoantipipipipipipine 0.31 mmol/l; Phenol 5.2 mmol/l; Cholesterol esterase ≥ 0.2 ku/l (3.3 μkat/l); Cholesterol oxidase ≥ 0.2 ku/l (3.3 μkat/l); Peroxidase ≥ 10 ku/l (166.7 μkat/l);
- Method: Enzymatic; Linear range: about 0.5 - 18.0 mmol/l (20 - 700 mg/dl); The wavelength is about 540 nm; Sample type: serum, plasma; CV ≤ 3% of the total bustle: CV ≤ 3%; Minimum number of tests/1 ml: 22 Test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x45ml |
||
44 |
Cholesterol quantitative testing reagent |
40 |
Box |
- Ingredients: Phosphate buffer solution (pH 6.5) 103 mmol/l; 4-aminoantipipipipipipine 0.31 mmol/l; Phenol 5.2 mmol/l; Cholesterol esterase ≥ 0.2 ku/l (3.3 μkat/l); Cholesterol oxidase ≥ 0.2 ku/l (3.3 μkat/l); Peroxidase ≥ 10 ku/l (166.7 μkat/l);
- Method: Enzymatic; Linear range about 0.5 - 18.0 mmol/l (20 - 700 mg/dL); The wavelength is about 540 nm; Sample type: serum, plasma; CV ≤ 3% of the total bustle: CV ≤ 3%; Minimum number of tests/1 ml: 22 Test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x22.5ml |
||
45 |
CK-MB quantitative testing reagent |
18 |
Box |
- Ingredients: Imidazole buffer solution (pH 6.7) 100 mmol/l; Diadenosine-Pentaphosphate 0.01 mmol/l; Hexokinase (HK) ≥ 4 ku/l; EDTA 2 mmol/l; NADP 2 mmol/l; Glucose 20 mmol/l; G6P-DH ≥ 2.8 ku/l; Creatine phosphate 30 mmol/l; ADP 2 mmol/l; N-acetylcysteine 0.2 mmol/l; Mg-acetate 10 mmol/l; Activation of 26 mmol/l; AMP 5 mmol/l; Antibodies resistant to ck-M;
- Method: Inhibit immunosuppressure; Linear range: about 10 - 2000 U/L (0.17 - 33.33 μkate/l); The wavelength is about 340 nm; Sample type: serum, plasma; Repeated level: CV ≤ 5%; Total bust: CV ≤ 6.5%; The minimum number of tests/1 ml: 6 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2x22ml+2x4ml+2x6ml |
||
46 |
Creatinin quantitative testing reagent |
75 |
Box |
- Ingredients: 120 mmol sodium hydroxide/l; Picric acid 2.9 mmol/l;
- Method: Jaffé Method; Linear range: Serum/plasma: Method A: about 5 - 2200 μmol/l (0.06 - 25.0 mg/dl); Method B: about 18 - 2200 μmol/l (0.2 - 25.0 mg/dl), urine: about 88 - 35360 μmol/l (1 - 400 mg/dl); Wavelength: about 520 nm; Sample type: serum, plasma, urine; Repeated level: CV ≤ 3%; Total bust: CV ≤ 5%; The minimum number of tests/1 ml: 4 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x51ml+4x51ml |
||
47 |
Ammonia quantitative test reagent |
55 |
Box |
- Ingredients: A1 reagent contains sodium tetraborate 30 mmol/l, preservatives, pH 9.3; A2 reagent contains sodium tetraborate 30 mmol/l, NADPH 0.24 mmol/l, after re -rehabilitation; Rate B contains 400 mmol/l, 2-oxoglutarat 22 mmol/l, glutamat dehydrogenase ≥ 320 U/ml, preservatives, pH 7;
- Method: spectrum, glutamate dehydrogenase; Sample type: plasma; Detection limit: 13 µmol/l (22 µg/dl); Linear limit: about 600 µmol/l (1022 µg/dl); Repeated level: CV ≤ 3%; Total bust: CV ≤ 4%
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: box 1 bottle of freezing powder (volume after tunnel 20 ml) + 1 bottle of 20 ml tunnel solution + 1 bottle of 7 ml solution |
||
48 |
Live bilirubin quantitative testing reagent |
5 |
Box |
- Ingredients: 3.5 dichlorophenyl diazonium tetrafluoroborate 0.08 mmol/l;
- Method: DPD; The measuring range is about 0.9 - 171 μmol/l (0.05 - 10 mg/dl); The wavelength is about 570 nm; Sample type: serum, plasma; Repeated level: CV ≤ 5%; Total bust: CV ≤ 7.5%; Minimum number of tests/1 ml: 16 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x20ml+4x20ml |
||
49 |
GGT quantitative test reagent |
55 |
Box |
- Ingredients: glycylglycine, pH 7.7 (37 ° C) 150 mmol/l; L-γ-Glutamyl-3-Carboxy-4-Nitroanilide 6 mmol/l;
- Method: Based on IFCC's recommendations; Linear range is about 5 - 1200 U/l (0.08 - 20,00 μkate/l); The wavelength is about 410 nm; Sample type: serum, plasma; Repeated level: CV ≤ 5%; Total bust: CV ≤ 10%; The minimum number of tests/1 ml: 3 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x40ml+4x40ml |
||
50 |
Glucose quantitative test reagent |
50 |
Box |
- Ingredients: Pipes buffer solution (pH 7.6) 24 mmol/l; ATP ≥ 2 mmol/l; NAD+ ≥ 1.32 mmol/l; Mg2+ 2.37 mmol/l; Hexokinase ≥ 0.59 ku/l; G6P-DH ≥ 1.58 ku/l;
- Method: Enzymatic (Hexokinase Method); Linear range: Serum/ plasma/ cerebrospinal fluid: about 0.6 - 45.0 mmol/ l, urine: about 0.2 - 45 mmol/ l; The wavelength is about 340 nm; Sample type: serum, plasma, urine and cerebrospinal fluid; Repeated level: CV ≤ 3%; Total bust: CV ≤ 5%; The minimum number of tests/1 ml: 13 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x53ml+4x27ml |
||
51 |
Glucose quantitative test reagent |
20 |
Box |
- Ingredients: Pipes buffer solution (pH 7.6) 24 mmol/l; ATP ≥ 2 mmol/l; NAD+ ≥ 1.32 mmol/l; Mg2+ 2.37 mmol/l; Hexokinase ≥ 0.59 ku/l; G6P-DH ≥ 1.58 ku/l; - Method: Enzymatic (Hexokinase Method); Linear range: Serum/ plasma/ cerebrospinal fluid: about 0.6 - 45.0 mmol/ l, urine: about 0.2 - 45 mmol/ l; Wavelength: about 340 nm; Sample type: serum, plasma, urine and cerebrospinal fluid; Repeated level: CV ≤ 3%; Total bust: CV ≤ 5%; The minimum number of tests/1 ml: 13 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x25ml+4x12.5ml |
||
52 |
Rate, calibration of HBA1C quantitative testing |
3 |
Box |
- Ingredients: + HBA1C R1 Antibody reagent: HBA1C antibody in humans (sheep) ≥ 0.5 mg/ml; MES 0.025 mol/l cushion, 0.015 mol/l buffer; + HBA1C R2 Polyhapt MES 0.025 mol/l cushion, 0.015 mol/l buffer; + Full hemoglobin R1: Phosphate cushion, pH 7.4: 0.02 mol/l;
- Method: THB: Measuring color A1C: Immunosuppressure measurement of turbidity; Linear range: THB: about 3.7–13.0 mmol/l (6–21g/dl) and HBA1C: 0.19 mmol/l (0.3 g/dl) to the concentration of calibration 6, % HBA1C: about 4 - 15 % HBA1C (NGSP); Wavelength: THB: 570 Nm HBA1C: 340 nm; Sample type: total blood; Repeat level: CV ≤ 4%; Total bust: CV ≤ 4%; The minimum number of tests/1 ml: 2 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2 x 37.5 ml + 2 x 7.5 ml + 2 x 34.5 ml + 5 x 2 ml |
||
53 |
HDL-Cholesterol quantitative testing reagent |
100 |
Box |
- Ingredients: antibodies β-lipoprotein in humans; Cholesterol esterase (cover) 0.8 IU/ml; Cholesterol oxidase (for) 4.4 IU/ml; Peroxidase (POD) 1.7 IU/ml; Ascorbate oxidase 2 IU/ml; Good's buffer solution (pH 7) 30 mmol/l; N-Ethyl- N- (2-Tydroxy-3-Sulfopropyl)- 3.5- Dimethoxy- 4 Fluoroaniline (F-DaOS) 0.2 mmol/l; 4-Aminoantipipipipipipine 0.67 mmol/l;
- Method: Enzymatic; Linear range: about 0.05 - 4.65 mmol/l (2 -180 mg/dl); Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 4.0%; The minimum number of tests/1 ml: 4 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x51.3ml+4x17.1ml |
||
54 |
HDL-Cholesterol quantitative testing reagent |
50 |
Box |
- Ingredients: antibodies β-lipoprotein in humans; Cholesterol esterase (cover) 0.8 IU/ml; Cholesterol oxidase (for) 4.4 IU/ml; Peroxidase (POD) 1.7 IU/ml; Ascorbate oxidase 2 IU/ml; Good's buffer solution (pH 7) 30 mmol/l; N-Ethyl- N- (2-Tydroxy-3-Sulfopropyl)- 3.5- Dimethoxy- 4 Fluoroaniline (F-DaOS) 0.2 mmol/l; 4-Aminoantipipipipipipine 0.67 mmol/l;
- Method: Enzymatic; Linear range: about 0.05 - 4.65 mmol/l (2 -180 mg/dl); Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 4.0%; The minimum number of tests/1 ml: 4 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x27ml+4x9ml |
||
55 |
Testing test reagent (calcium) |
12 |
Box |
- Ingredients: Imidazol (pH 6.9); Arsenazo III 0.02%;
- Method: Arsenazo III; Linear range: serum, plasma: about 1 - 5 mmol/l (4 - 20 mg/dl); Urine: about 0.1 - 10 mmol/l (0.4 - 40 mg/dl); Wavelength: about 660 nm; Sample type: serum, plasma, urine; Repeatedly ≤3%; Total bust: ≤ 4%; The minimum number of tests/1 ml: 32 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x29ml |
||
56 |
Fe (iron) quantitative test reagent |
2 |
Box |
- Ingredients: Glycin cushion (pH 1,7) 215 mmol/l; L-ASCORBIC Acid 4.7 mmol/l; 2,4,6-Tri (2-Pyrylyl) -5-Triazine 0.5 mmol/l;
- Method: TPTZ; Linear range: about 2 - 179 μmol/l (10 - 1000 μg/dl); Wavelength: about 600 nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 5.0%; The minimum number of tests/1 ml: 10 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x15ml+4x15ml |
||
57 |
Fe (iron) quantitative test reagent |
3 |
Box |
- Ingredients: Glycin cushion (pH 1,7) 215 mmol/l; L-ASCORBIC Acid 4.7 mmol/l; 2,4,6-Tri (2-Pyrylyl) -5-Triazine 0.5 mmol/l;
- Method: TPTZ; Linear range: about 2 - 179 μmol/l (10 - 1000 μg/dl); Wavelength: about 600 nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 5.0%; The minimum number of tests/1 ml: 9 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x30ml+4x30ml |
||
58 |
IVD Buffer in quantitative tests Na, K, CL |
35 |
Box |
Buffer solution used for quantitative tests (indirect) concentrations Na+, K+ and Cl-;
Ingredients: triethanolamine ≤ 0.1 mol/l
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x2000ml |
||
59 |
Calibration agent average quantitative test Na, K, CL |
42 |
Box |
The average calibration is used for quantitative tests (indirect) concentrations Na+, K+ and Cl-;
Ingredients: Na+ 4.3 mmol/l; K+ 0.13 mmol/l; Cl- 3.1 mmol/l
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x2000ml |
||
60 |
IVD creates basic voltage for quantitative tests Na, K, CL |
18 |
Box |
Electrolyte chemicals for reference electrodes used for quantitative (indirect) testing of Na+, K+ and Cl- concentrations;
Ingredients: Potassium chloride ≤ 1 mol/L
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x1000ml |
||
61 |
Lactat quantitative testing reagent |
35 |
Box |
- Ingredients: Lactate oxidase ≥ 0.2 kU/L; Peroxidase ≥ 1 kU/L; Good’s Buffer (pH 7.0) 50 mmol/L; 4-aminoantipyrine 0.1 mmol/L; TOOS ≥ 0.3 mmol/L; N-ethyl-N-(2-hydroxy-3-sulfopropyl)-3-methylaniline;
- Method: Enzymatic; Linear range: approximately 0.22 – 13.32 mmol/L (2 – 120 mg/dL); Sample type: Plasma, cerebrospinal fluid; Repeatability: CV ≤ 5.0%; Overall precision: CV ≤ 5.0%;
- Minimum number of tests/1 mL: 4 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x10ml + 4xlyo |
||
62 |
LDH quantitative test reagent |
3 |
Box |
-Ingredients: d (-) n-methylglucamin buffer, pH 9.4 (37 ° C) 325 mmol/l; Lactate 50 mmol/l; NAD+ 10 mmol/l;
- Method: Based on IFCC's recommendations; Linear range: about 25–1200 U/l (0.4–20 µKat/l); Wavelength: about 340nm; Sample type: serum, plasma; Repeated level: CV ≤ 5.0%; Total bust: CV ≤ 10.0%;
- Minimum number of tests/1 ml: 8 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x40ml+4x20ml |
||
63 |
LDL-CHOLesterol quantitative testing reagent |
135 |
Box |
- Ingredients: Cholesterol esterase 3.7 IU/ml; Cholesterol oxidase 3.7 IU/ml; Peroxidase 4.9 IU/ml; Sodium Azit 0.1%; Good buffer solution (pH 6.8) 25 mmol/l; 4-Aminoantipipipipipipine 0.8 mmol/l; Catalase 743 IU/ml; HDAOS 0.47 mmol/l;
- Method: Enzymatic; Linear range: about 0.26 - 10.3 mmol/l (10 - 400 mg/dl); Wavelength: about 600 nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 4.0%;
- Minimum number of tests/1 ml: 4 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x51.3ml+4x17.1ml |
||
64 |
LDL-CHOLesterol quantitative testing reagent |
60 |
Box |
- Ingredients: Cholesterol esterase 3.7 IU/ml; Cholesterol oxidase 3.7 IU/ml; Peroxidase 4.9 IU/ml; Sodium Azit 0.1%; Good buffer solution (pH 6.8) 25 mmol/l; 4-Aminoantipipipipipipine 0.8 mmol/l; Catalase 743 IU/ml; HDAOS 0.47 mmol/l;
- Method: Enzymatic; Linear range: about 0.26 - 10.3 mmol/l (10 - 400 mg/dl); Wavelength: about 600 nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 4.0%;
- Minimum number of tests/1 ml: 4 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x27ml+4x9ml |
||
65 |
RF quantitative test reagent |
6 |
Box |
- Ingredients: Glycine Buffer (pH 8.0) 170 mmol/l; Latex covered with human IgG <0.5%;
- Method: Measure immunity; Linear range: about 10–120 IU/ml; Sample type: serum, plasma; Repeated level: CV ≤ 10.0% of the total bust: CV ≤ 10.0%;
- Minimum number of tests/1 ml: 6 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x24ml+4x8ml |
||
66 |
Total bilirubin quantitative testing reagent |
1 |
Box |
- Ingredients: Caffeine 2.1 mmol/L; 3.5 Dichlorophenyl diazonium tetrafluoroborate 0.31 mmol/L; Surfactants;
- Method: DPD; Linear range: approximately 0.5–513 µmol/L (0.03–30 mg/dL); Wavelength: about 540nm; Sample type: Serum, plasma; Repeatability: CV ≤ 3.0%; Overall precision: CV ≤ 5.0%;
- Minimum number of tests/1 mL: 16 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x40ml+4x40ml |
||
67 |
Total bilirubin quantitative testing reagent |
3 |
Box |
- Ingredients: caffeine 2.1 mmol/l; 3.5 Dichlorophenyl diazonium tetrafluoroborate 0.31 mmol/l; Surfactants;
- Method: DPD; Linear range: about 0.5–513 µmol/l (0.03–30 mg/dL); Wavelength: about 540nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 5.0%;
- Minimum number of tests/1 ml: 16 Test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x15ml+4x15ml |
||
68 |
Total protein quantitative testing reagent |
2 |
Box |
- Ingredients: Sodium hydroxyd 200 mmol/l; Potassium sodium tartrat 32 mmol/l; Copper sulphat 18.8 mmol/l; Potassium iodid 30 mmol/l;
- Methods: optical measurement; Linear range: about 30–120 g/l (3–12 g/dl); Wavelength: about 540nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 4.0%;
- Minimum number of tests/1 ml: 10 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x48ml+4x48ml |
||
69 |
Total protein quantitative testing reagent |
4 |
Box |
- Ingredients: Sodium hydroxyd 200 mmol/l; Potassium sodium tartrat 32 mmol/l; Copper sulphat 18.8 mmol/l; Potassium iodid 30 mmol/l;
- Method: photometric; Linear range: about 30–120 g/l (3–12 g/dl); Wavelength: about 540nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 4.0%;
- Minimum number of tests/1 ml: 10 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x25ml+4x25ml |
||
70 |
Triglyceride quantitative testing reagent |
65 |
Box |
-Ingredients: PIPES buffer (pH 7.5) 50 mmol/L; Mg2+ 4.6 mmol/L; MADB 0.25 mmol/L; 4-Aminoantipyrine 0.5 mmol/L; ATP 1.4 mmol/L; Lipases 1.5 kU/L (25 μkat/L); Glycerol kinase 0.5 kU/L (8.3 μkat/L); Peroxidase 0.98 kU/L (16.3 μkat/L); Ascorbate oxidase 1.48 kU/L (24.6 μkat/L); Glycerol-3-phosphate oxidase 1.48 kU/L (24.6 μkat/L);
- Method: Enzyme; Linear range: approximately 0.1 – 11.3 mmol/L (10 – 1000 mg/dL); Wavelength: about 660 nm; Sample type: Serum, plasma; Repeatability: CV ≤ 3.0%; Overall precision: CV ≤ 5.0%;
- Minimum number of tests/1 mL: 8 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x50ml+4x12.5ml |
||
71 |
Triglyceride quantitative testing reagent |
30 |
Box |
- Ingredients: Pipes cushion (pH 7.5) 50 mmol/l; Mg2+ 4.6 mmol/l; Madb 0.25 mmol/l; 4-Aminoantipipipipipipine 0.5 mmol/l; ATP 1.4 mmol/l; Lipases 1.5 ku/l (25 μkat/l); Glycerol kinase 0.5 ku/l (8.3 μkat/l); Peroxidase 0.98 Ku/L (16.3 μkat/l); Ascorbate oxidase 1.48 Ku/L (24.6 μkat/l); Glycerol-3-phosphate oxidase 1.48 ku/l (24.6 μkate/l);
- Method: enzyme; Linear range: about 0.1 - 11.3 mmol/l (10 - 1000 mg/dL); Wavelength: about 660 nm; Sample type: serum, plasma; Repeated level: CV ≤ 3.0%; Total bust: CV ≤ 5.0%;
- Minimum number of tests/1 ml: 8 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x20ml+4x5ml |
||
72 |
URE quantitative testing reagent |
50 |
Box |
- Ingredients: "Tris 100 mmol/l; nadh ≥ 0.26 mmol/l; tetra sodium diphosphate 10 mmol/l; edta 2.65 mmol/l; 2-olglutarat ≥ 9.8 mmol/l; urease ≥ 17.76 ku/l; ADP ≥ 2.6 mmol/l; gldh ≥ 0.16 ku/l ; Tinning strip: Serum, plasma: about 5–300 mg/dl (0.8–50.0 mmol/l) urine: about 60–4500 mg/dl (10-750 mmol/l);
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x53ml+4x53ml |
||
73 |
URE quantitative testing reagent |
20 |
Box |
- Ingredients: "100 mmol/l buffer; nadh ≥ 0.26 mmol/l; tetra sodium diphosphate 10 mmol/l; edta 2.65 mmol/l; 2-oxoglutarat ≥ 9.8 mmol/l; urease ≥ 17.76 ku/l; ADP ≥ 2.6 mmol/l;
- Methods: GLDH, Measuring Mobile UV; Linear range: serum, plasma: about 5–300 mg/dL (0.8–50.0 mmol/l) urine: about 60–4500 mg/dL (10-750 mmol/l); Sample type: serum, plasma, urine; Repeated level: CV ≤ 5%; The whole bumping CV ≤ 10%;
- Minimum number of tests/1 ml: 10 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x25ml+4x25ml |
||
74 |
Uric acid quantitative test reagent |
25 |
Box |
- Ingredients: Phosphate cushion (pH 7.5) 42 mmol/l; Madb 0.15 mmol/l; 4-Aminophenazon 0.30 mmol/l; Peroxidase ≥ 5.9 KU/L (98 μkat/l); Uricase ≥ 0.25 ku/l (4.1.15 μkat/l); Ascorbat oxidase ≥ 1.56 ku/l (26 μkat/l);
- Method: Uricase; Linear range: serum, plasma: about 1.5–30 mg/dl (89–1785 μmol/l), urine: about 2–400 mg/dl (119–23800 μmol/l); Wavelength: about 660nm; Sample type: serum, plasma, urine; Repeated level: CV ≤ 3%; Total bust: CV ≤ 5.0%;
- Minimum number of tests/1 ml: 11 Test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x42.3ml+4x17.7ml |
||
75 |
Albumin quantitative testing reagent |
50 |
Box |
- Ingredients: 18 mmol/l mocphat cushion; Antibodies (goats) resistant to human albumin; Polyethylene Glycol 8000 3.6%; Sodium Azit <0.1% (W/W);
- Method: Measure immunity; Measuring range: Urine: about 0.7–45 mg/dl (7–450 mg/l); Cerebrospinal fluid: about 1–45 mg/dL (10–450 mg/l); Wavelength: about 380nm; Sample type: urine, cerebrospinal fluid; Repeated level: CV ≤ 5%; Total bust: CV ≤ 10%; The minimum number of tests/1 ml: 3 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x32.6ml+4x4.4ml |
||
76 |
Α-Amylase quantitative testing reagent |
5 |
Box |
- Ingredients: MES (pH 6.05) 36.1 mmol/l; Calcium acetate 3.60 mmol/l; NaCl 37.2 mmol/l; Potassium Thiocyanate 253 mmol/l; CNPG3 1.63 mmol/l;
- Method: CNPG3; Linear range: Serum/plasma: about 10 - 2000 U/l (0.2 - 33.3 μkate/l), urine: about 5 - 4800 U/L (0.1 - 80 μkate/l); Wavelength: about 410 nm; Sample type: serum, plasma, urine; Repeated level: CV ≤ 5.0%; Total bust: CV ≤ 10.0%; The minimum number of tests/1 ml: 5 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x40ml |
||
77 |
CRP quantitative test reagent |
27 |
Box |
- Ingredients: Glycine buffer 100 mmol/l; Latex, coated antibody CRP ≤ 0.5% W/V;
- Method: immune measurement of turbidity; Linear range: Normal application: about 0.2–480 mg/l, high sensitivity application: about 0.08–80 mg/l; Sample type: serum, plasma; Repeated level: CV ≤ 6%; Total bust: CV ≤ 10%; The minimum number of tests/1 ml: 3 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x30ml+4x30ml |
||
78 |
Ethanol quantitative test reagent |
15 |
Box |
- Ingredients: Rate A contains 100 mmol/l pipes cushion, preservatives, pH 7.9; Rate B contains 50 mmol/l pipes cushion, nad 15 mmol/l, alcohol dehydrogenase (ADH) ≥ 18 ku/l, preservatives, pH 6.2;
- Method: spectrum, alcohol dehydrogenase; Sample type: serum, plasma, urine; Detection limits: 8.11 mg/dL (1.76 mmol/l); Linear limit: about 300 mg/dl (65.1 mmol/l); Repeated level: CV ≤ 3.5%; Total bust: CV ≤ 4.5%
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2x20ml+2x7ml |
||
79 |
Homocystein quantitative testing reagent |
30 |
Box |
-Ingredients: containing s-adenosylmethionin (sam) 0.01 mm, nadh ≥ 0.2 mm, tcep≥ 0.5 mm, 2-oxoglutarat 5.0 mm, glutamat dehydrogenase 10 ku/l, hydrolase sah 3.0 ku/l, adenosin deaminase 5.0 ku/l, hcy methyltransferase 5,0 ku/l;
- Method: UV, 2 -point dynamic measurement (fixed), enzyme cycle (enzymatic cycling); Sample type: serum, plasma; Measurement range: about 3 - 50 µmol/l; Detection limit: about 0.4 µmol/l; Repeated level: CV ≤ 5%; Total values: CV ≤ 6%
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 3x20ml R1,1x18ml R2 |
||
80 |
Procalcitonin quantitative test (PCT) |
105 |
Box |
- Procalcitonin quantitative test (PCT) in serum and plasma on automatic immune testing machines;
- Method: immunity enzyme two consecutive steps ("sandwich"); Measurement range: approximately from 0.01–100 ng/ml;
- Main ingredients: The agreed particles from single -line antibodies (mice) Procalcitonin in the buffer solution have surfactants, proteins (cows), sodium azid, proclin 300, sodium hydroxid, a combination of alkaline alkaline phosphate recombinant with antibodies (mouse) antibodies (Procalcitonin) in mops buffer solution
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2x 50 test |
||
81 |
Magnesi quantitative test reagent |
30 |
Box |
-Ingredients: Acid ∈-Amino-N Caproic 450 mmol/l; 100 mmol/l; Acid glycoletherdiamine-n, n, n ', n' tetraacetic 0.12 mmol/l; XYLISLIL 0.18 mmol/l;
- Method: Xuclididyl; Linear range: serum, plasma: about 0.2–3.3 mmol/l (0.5–8.0 mg/dl); Urine is about 0.2 - 7.8 mmol/l (0.5 - 18.9 mg/dL); Wavelength: about 520nm; Sample type: serum, plasma, urine; CV repeatedly ≤ 3.0%; The whole bumping CV ≤ 5.0%; The minimum number of tests/1 ml: 5 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x40ml |
||
82 |
Run reagent, calibration quality testing total protein |
12 |
Box |
- Ingredients: R1: Pyrogallol red 47 μmol/l; Sodium molybdat 320 μmol/l; Succinic acid 50 mmol/l; Sodium benzoate 3.5 mmol/l; 1 mmol/l sodium oxalate; 0.8% w/v methanol; Calibration substance: albumin serum 0.5 g/l;
- Method: red pyrogallol molybdat; Linear range: about 0.01–2 g/l; Wavelength: about 600nm; Sample type: urine, cerebrospinal fluid; Repeated level: CV ≤ 5.0%; Total bust: CV ≤ 10.0%; The minimum number of tests/1 ml: 5 tests
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x19ml+1x3ml |
||
83 |
Inorganic quantitative test p (phosphorus) |
10 |
Box |
-Part: Sulfuric acid 200 mmol/l; Ammoniumheptamolybdate 0.35 mmol/l; Glycine 50 mmol/l;
- Method: UV optical measurement; Linear range: Serum is about 0.32–6.4 mmol/l (1–20 mg/dl); Urine: about 3 - 113 mmol/l (9.3 - 350 mg/dl); Sample type: serum, plasma, urine; Repeated level: CV ≤ 3%; Total bust: CV ≤ 5%; Minimum number of tests/1 ml: 16 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x15ml+4x15ml |
||
84 |
Inorganic quantitative test p (phosphorus) |
5 |
Box |
- Ingredients: 200 mmol/l sulphuric acid; Ammoniumheptamolybdate 0.35 mmol/l; Glycine 50 mmol/l;
- Method: UV optical measurement; Linear range: Serum is about 0.32–6.4 mmol/l (1–20 mg/dl); Urine: about 3 - 113 mmol/l (9.3 - 350 mg/dl); Wavelength: about 340 nm; Sample type: serum, plasma, urine; Repeated level: CV ≤ 3%; Total bust: CV ≤ 5%; Minimum number of tests/1 ml: 16 test
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 4x40ml+4x40ml |
||
85 |
Vitamin B12 quantitative test reagent |
25 |
Box |
- Quantitative testing of vitamin B12 in serum and heparin (heparin) on automatic immune testing machines;
- Method: Enzyme immunity is competitive; Measurement range: approximately 50-1500 PG/ml [37-1107 PMOL/L];
- Main ingredients: Thuan seeds from antibody complex (goat) resistant to mouse IgG - antibody (mouse, single line) resistant to the intrinsic element, Tris cushion salts, surfactants, albumin of cow serum (BSA), sodium azid and procline, borate cushions, cobinamid, added substance inner factors (pigs) - alkali phosphate (cow), NaOH solution (NaOH) 0.005% potassium cyanide (KCN), 0.02% acetic acid solution with dithiothreitol (DTT)
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box: 2x50test |
||
86 |
Test reagents determine prothrombin time (PT) and quantify fibrinogen |
60 |
Box |
- Chemicals with average ISI sensitivity reaches about 1.00. The linear level with a minimum fibrinogen is 60 - 700 mg/dL. Dry powder and preservatives and cushions.
- Minimum component containing: Factors of recombinant tissue, synthetic phospholipid, calcium chloride. Stability used after reconstitution (or open the lid) minimum 10 days at 2-8 degrees Celsius and at least 10 days at 15 degrees Celsius on the machine.
- Certificate of CE, ISO quality (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
5 x 20 ml+5 x 20 ml |
||
87 |
Test reagents determine prothrombin time (PT) and quantify fibrinogen |
25 |
Box |
- Chemicals with an average ISI sensitivity of 1.00. Linearity with Fibrinogen is at least about 60 - 700 mg/dL. Dry powder and preservatives and buffers.
- Minimum ingredients contain: recombinant human tissue factor, synthetic phospholipids, calcium chloride. Stability after reconstitution (or opening) is at least 10 days at temperatures from 2-8 degrees Celsius and at least 4 days at 15 degrees Celsius on the machine.
- CE, ISO quality certification (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
5 x 8 ml+5 x 8 ml |
||
88 |
Testing reagents determine APTT time |
60 |
Box |
- Test time APTT packaging with calcium chloride. Liquid form.
- The minimum ingredient contains silica glue, synthetic phospholipid, cushion and preservatives. Stability used after reconstitution (or open the lid) at least 30 days of temperature 2-8 degrees Celsius, at least 10 days of temperature 15 degrees Celsius on the machine.
- Certification of CE, FDA, ISO quality (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
5 x10 ml+5 x10 ml |
||
89 |
Fibrinogen quantitative testing reagent |
60 |
Box |
- Fibrinogen-Clauss quantitative test, performed on blood clotting testing machines. Dry powder.
- Minimum component containing: Thrombin originating from cow. Linear linearity is at least 35 mg/dL and up to 1000 mg/dL. Stability used after reconstitution (or open the lid) minimum at least 7 days of temperature 2-8 degrees C, at least 7 days of temperature 15 degrees Celsius on the machine. Certification CE, FDA, ISO (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
10 x 5 ml |
||
90 |
Fibrinogen quantitative testing reagent |
25 |
Box |
- Fibrinogen-Clauss quantitative test. Dry powder.
- Minimum component containing: Thrombin originating from cow. Linear linearity is about 35 mg/dL and maximum of about 1000 mg/dL. Stability used after reconstitution (or open lid) minimum at least 3 days of temperature from 2-8 degrees Celsius, at least 3 days of temperature 15 degrees Celsius on the machine. Packaging: 20 ml (or equivalent)
- Certification of CE, FDA, ISO quality (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
10 x2 ml |
||
91 |
Testing cards identify sensitive red blood cells, abnormal antibodies, blood transfusion and antigen |
25 |
Box |
Gel Card ≥ 8 wells, cards are used in direct and indirect globulin resistance tests on human blood samples in gel technique. Tests include screening and identifying abnormal antibodies, cross -reaction, self -control and classification of red blood cells.
Minimum component: solution with low I-density with cushioning agents (liss) with human globulin resistance; A mixture of multi -line anti -IgG antibodies and single -line C3D antibodies.
The test is performed manually or on automatic blood type analyzer. Storage: 2 to 25 degrees Celsius: ≥ 50 cards/box certification box FDA, CE, ISO (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
2x25 cards |
||
92 |
Dilute solution for hematological tests |
1.700 |
Box |
The diluted solution (isomorphic cushion) is used in combination with the agent in the test to count and size the blood cells on the automatic cell analysis system.
Minimum component: Imidazole, does not contain stable cyanide: minimum 60 days of ISO quality certification (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
10L |
||
93 |
IVD Red blood cell solution in hematology test |
68 |
Box |
The red blood cell solution is used for hemoglobin quantitative testing, determining the number of NRBC, counting and sizes of white blood cells on automatic cell testing machines.
Maximum composition: Quatnary ammonium salts, sodium sulfite stability after opening: minimum 60 days of ISO quality certification (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
5L |
||
94 |
IVD Red blood cells and white blood cell protection in hematology tests |
110 |
Box |
Chemicals of red blood cells and protective leukocytes to create testing tests (minimum 5 components) with technology integrated measurement methods (volume, conductivity, multi -channel scattering) on automatic cell analyzer system.
Ingredients include chemicals of red blood cells and white blood cell stabilization, at least containing formic acid, sodium carbonate stability after opening: minimum 60 days of ISO quality certification (13485)
(or equivalent) |
S.I.S International General Hospital Can Tho |
1900ml+850ml |
||
95 |
Rate, calibration of D-Dimer quantitative testing |
160 |
Box |
D-Dimer quantitative testing standard;
Ingredients: H people (or equivalent) |
S.I.S International General Hospital Can Tho |
3x4 ml + 3x6 ml + 2x1 ml |
||
96 |
The column contains HBA1C testing chemicals by HPLC method |
35 |
Box |
The column contains HBA1C testing chemicals used to quantify the components of HBA1C by ion exchange chromatography method.
- Ingredients: Chromatographic column: Hydrophilic polymer of methacrylate esters copolymer, integrated filter set.
- ISO 13485 standard.
- Packing: 4000 tests/ unit/ box
(or equivalent) |
S.I.S International General Hospital Can Tho |
4000 test/ 1 unit/ box |
||
97 |
Wash solution before A0 and durable chromatography column |
150 |
Box |
The washing solution in front of A0 and durable chromatography columns is used to determine the amount of HBA1C in the whole blood sample of the person.
- Ingredients: Sodium perchlorate concentration ≤ 1%; Sodium Azide concentration ≤ 0.1%
- PH: 5.2 - 5.5
- Quality standard: ISO 13485.
- Packing: 600 ml x 4/ box
(or equivalent) |
S.I.S International General Hospital Can Tho |
600ml x4 /box |
||
98 |
Wash solution before A0 and HB variant (HBC) |
115 |
Box |
The washing solution before A0 and HB variant (HBC) is used to determine the amount of HBA1C in the whole blood sample of the person.
- Ingredients: Sodium perchlorate concentration: from 1-5%; Phosphate concentration: ≤ 2.0%; Sodium Azide concentration: ≤ 0.1%.
- PH: From 7.7 - 8.3
- Quality standard: ISO 13485.
- Packing: 600ml x 2/ box
(or equivalent) |
S.I.S International General Hospital Can Tho |
600ml x2 /box |
||
99 |
Washing solution before A0 and HB variant (HBS) |
210 |
Box |
A0 pre-eluent and Hb variant (HbS) were used to determine the amount of HbA1c in human whole blood samples.
- Ingredients: Phosphate concentration ≤ 2%; Sodium perchlorate concentration ≤ 0.3%; Sodium azide concentration ≤ 0.1%
- pH: from 6.8 - 7.3
- Quality standards: ISO 13485.
- Packaging: 600ml x 2/ Box
(or equivalent) |
S.I.S International General Hospital Can Tho |
600ml x2 /box |
||
100 |
The solution dilute the whole blood sample when testing HBA1C |
195 |
Box |
The solution dilute the whole blood sample when the HBA1C test is used to determine the A1C hemoglobin (HBA1C) in the human whole blood sample. Used to dilute whole blood samples and clean the pipes where the sample flows.
Ingredients: 2- Phenoxyethanol concentration ≤ 1%; Sodium Azide concentration ≤ 0.02%
- PH: 7.3 - 7.7
- Quality standard: ISO 13485
- Packaging: 2l x 3/ Box
(or equivalent) |
S.I.S International General Hospital Can Tho |
2000ml x3 /box |
||
101 |
Calibration
Measurement test
pH, electrolytes,
HCT |
12 |
Box |
Purpose of use of chemicals:
+ Provide standard points for pH calibration, electrolyte and hematocrit. The limit pH buffer is cushioned to the pH 7.382 at 37 ° C
+ Provide slope points for pH calibration and 2 -point electrolyte. The limit pH buffer is cushioned to the pH of 6,838 at 37 ° C
Each set includes: 370ml of 7.382 cushion chemicals to be cushioned to pH 7.382 and 90ml of 6,838 cushioned chemicals to be cushioned to 6,838 pH. Ingredients: 100mm m0ps/Na mpos, salt, surfactant substance, preservatives.
(or equivalent) |
S.I.S International General Hospital Can Tho |
4 Sets/ Box (460mlx4) |
||
102 |
Solution
wash machine
gas
Blood, electricity
prize |
12 |
Box |
Wash the probe and the sample path. Each set of 450ml of chemicalscogs includes salt, surface copper active, preservatives.
(or equivalent) |
S.I.S International General Hospital Can Tho |
4 sets/ box (450mlx4) |
||
103 |
Combiscreen 11 Auto |
600 |
Box |
- Specifications: Measuring 11 urine parameters including: glucose, pH, protein, blood, ketones, nitrite, bilirubin, urobilinogen, density, leukocytes, Ascorbic acid.
-Ascorbic acid reagent ingredient: 2.6-dichlorophenolindophenol 0.7 % bilirubin: Diazonium salt 3.1 % blood: tetramethylbenzidine-dihydrochloride 2.0 %, isopropylbenzol-hygroperoxide 21.0 % glucose: glucose oxid Peroxidase 0.9 %; Otolidine-Hydrochloride 5.0 % Ketones: Sodium Nitroprusside 2.0 % leukemia: Carboxylic acid ester 0.4 %; Diazonium Salt 0.2 % Nitrite: Tetrahydrobenzo [H] Quinolin-3-ol 1.5 %; Sulfanilic Acid 1.9 % pH: Methyl Red 2.0 %; Bromothymol Blue 10.0 % Protein: Tetrabromophenol Blue 0.2 % Density: Bromothymol Blue 2.8 % Urobilinogen: Diazonium Salt 3.6 %
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box of 150 test |
||
104 |
Main chemical test HBA1C |
75.000 |
kiểm TRA |
Perform glycated hemoglobin quantitative testing techniques according to high -pressure liquid chromatography (HPLC) by cation exchange method (column stuffed with very small serin plastic particles and no internal holes). The stable time of the chromatographic column mounted on the machine is to perform the expiry date of the chemical column on the packaging. HBA1C results are not interfered with HBF ≤ 30% and the presence of HBD, S, C or HBF heterozygous. Capacity of at least 60 samples/hour. CV ≤ 1%. CFS certificate. Chemicals are ready to use. FDA/CE standard and HBA1C testing method are standardized under the International Chemical and Clinical Federation (IFCC) and in accordance with the standards of the National Program on Standardization of Glycohemoglobin (NGSP-NATIONAL GlyCohemoglobin Standardization Program).
(or equivalent) |
S.I.S International General Hospital Can Tho |
1 column/ box (2500 test) |
||
105 |
HBA1C buffer solution No. 1. |
96.000 |
ML |
The number 1 buffer solution is used in a test tube, measuring Hemoglobin A1C (HBA1C) in total blood samples equal to the method of high -pressure liquid chromatography. Including organic acid solutions, each containing less than 0.05% sodium azide as preservatives. Storage & stability: When the lid has not been opened to the expiry date when the expiry date when stored from 4 to 30 ° C.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box/800ml |
||
106 |
HBA1C buffer solution No. 2 |
88.000 |
ML |
The buffer solution No. 2 is used in a test tube, measuring Hemoglobin A1C (HBA1C) in the total blood sample is equal to the high -pressure liquid chromatography method. Including: Organic acid solutions, each containing less than 0.05 % sodium Azide as preservatives. Storage & stability: When the lid has not been opened to the expiry date when the expiry date when stored from 4 to 30 ° C.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box/800ml |
||
107 |
HBA1C buffer solution No. 3. |
60.000 |
ML |
Buffer solution No. 3 is used in testing in test tubular, measuring hemoglobin A1C (HBA1C) in total blood samples equal to the method of high -pressure liquid chromatography. Including: Organic acid solutions, each containing less than 0.05 % sodium Azide as preservatives. Storage & stability: When the lid has not been opened to the expiry date when the expiry date when stored from 4 to 30 ° C.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box/800ml |
||
108 |
HBA1C solution and washing solution |
148.000 |
ML |
The solution contains ions, EDTA and triton X. Each type contains less than 0.1% sodium azide as preservatives. Storage & stability: When not open the lid is always stable until the expiry date when stored from 4 to 30 ° C. The expiry date is stated on the box and bottle label.
(or equivalent) |
S.I.S International General Hospital Can Tho |
Box/800ml |
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