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| No | List of product/services | Quantity | Unit | Description | Location | Specification | Note | Feature |
|---|---|---|---|---|---|---|---|---|
1 |
HBA1C quantitative testing reagent |
20 |
Box |
Method: Immune test measurement of latex turbidity
Normal reference value 0-16%
Main ingredients:
HBA1C R1 reagent
Latex.
Sodium Azide (0.95 g/l).
HBA1C R2 reagent
Antibody complex, single -line antibody antibodies hemoglobin A1C and anti -IgG antibodies mouse
Stable substance.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 4x20ml
R2: 2x10ml
Lysing: 2x100ml |
||
2 |
HBA1C quantitative testing materials |
50 |
Box |
HBA1C Test Quality Control Materials
Main ingredients: Human serum. Freezing form.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
L: 1x0.5ml
H: 1x0.5ml |
||
3 |
HBA1C quantitative quality calibration quality |
35 |
Box |
HBA1C quantitative test standard.
Main ingredients: Human serum.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
4x0.5ml |
||
4 |
HDL cholesterol quantitative testing reagent |
15 |
Box |
Method: Direct
Main ingredients:
R1:
Dextran sulfate ≤ 10 g/dl
Magnesium chloride hexahydrate ≤5 g/dl
Preservative
Brij 35≤ 10 g/dl
R2:
Detergent ≤ 2 %
PEG - Cholesterol esterase ≤5 ku/l
PEG - Cholesterol Oxidase≤5 Ku/L
4 aap≤ 1 g/dl
Peroxidase≤ 8000 U/L
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 3x50ml
R2: 2x25ml |
||
5 |
Quality control materials for HDL/LDL cholesterol quantitative test |
15 |
Box |
Quality control materials for HDL/LDL cholesterol quantitative tests.
To control the regular quality of HDL directly, LDL directly, Lipoprotein (A), Apolipoprotein A-1, Apolipoprotein B, Cholesterol and Triglyceride concentration.
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
|||
6 |
HDL cholesterol quantitative testing standard |
25 |
Jar |
HDL cholesterol quantitative testing standard
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
|||
7 |
LDL Cholesterol LDL test |
15 |
Box |
Method: Directly
Measurement range: 0.4 - 697mg/dl
Testing sensitivity is 0.03 mmol/l
Main ingredients:
R1:
Good’s buffer, pH 7.1: 50 mmol/l
Cholesterol oxidase: 500 U/L
Cholesterol esterase: 600 U/L
Catalase: 600 ku/l
Ascorbate oxidase: 3 ku/l
Toos: 2 mmol/l
R2:
Peroxidase: 4 ku/l
4-Aminoantipipipipine: 4 mmol/l
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 3x50ml
R2: 2x25ml |
||
8 |
LDL cholesterol quantitative test standard |
20 |
Jar |
LDL cholesterol quantitative test standard
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
|||
9 |
Triglyceride quantitative testing reagent |
25 |
Box |
Method: GPO-PAP (Glycerol Phosphate Oxidase/Peroxidase)
Ranking range: 0 - 1400 mg/dl
Detection limit: 0.5 mg/dL (0.05 mmol/l)
Main ingredients:
Pipes Buffer PH 7.0: 50 mmol/l
P-Chlorophenol: 2 mmol/l
Lipoprotein Lipase: 150000 U/L
Glycerolkinase: 800 U/L
Glycerol - 3 - P- oxidase: 4000 U/L
Peroxidase: 440 U/L
4-Aminoantipipipipine: 0.7mmol/l
ATP: 0.3mmol/l
Mg2+: 40 mmol/l
Na-cholate: 0.20 mmol/l
Potassium-hexacyanoferrat (II): 1µmol/l
Standard:
Triglycerides Standard (cat.: 208s): 200 mg/dl
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
6x65ml |
||
10 |
Test reagent diagnosed with uric acid |
7 |
Box |
Method: Uricase-PAP
Road measurement: 0-30 mg/dl
Detection limit: 0.2 mg/dl (11.9 µmol/l)
Main ingredients:
Phosphate buffer PH 8.0: 50 mmol/l
DHBSA*: 4 mmol/l
Uricase: 60 U/L
POD: 660 U/L
4-Aminoantipipipipine: 1 mmol/l
Preservative
Uric Acid Standard (Cat.: NO.: 499s): 6 mg/dl (356.9 μmol/l)
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
4x65ml |
||
11 |
Bilirubin Direct test reagent |
3 |
Box |
DCA method
Wavelength 546 nm (540 - 560 nm)
Optical road 1 cm
The measurement range from 0.05-23mg/DL
The detection limit is below 0.1 mg/dL.
Main ingredients:
R1: EDTA-NA2 0.1 mmol/l
NaCl 150 mmol/l
Sulfamic acid 100 mmol/l
R2: 2.4-Dichlorophenyl-Diazonium salt 0.5 mmol/l
HCl 900 mmol/l
Edta-na2 0.13 mmol/l
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 3x50ml
R2: 3x10ml |
||
12 |
Bilirubin Total test reagent |
3 |
Box |
Method: DCA
The measurement range from 0-30 mg/dL
The lower detection limit is 0.07 mg/dl.
Main ingredients:
R1: Phosphate buffer 50 mmol/l
NaCl 150 mmol/l
R2: 2.4-Dichlorophenyl-Diazonium Salt 5 mmol/l
HCl 130 mmol/l
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 3x65ml
R2: 3x14ml |
||
13 |
Cholesterol test reagent |
21 |
Box |
Method: ChoD-PAP (cholesterol oxidase/people)
Scope: 1.8 - 750mg/dl
Detection limit: 3 mg/dL (0.08 mmol/l)
Main ingredients:
R1: Pipes Buffer, pH 6.9: 90 mmol/l
Phenol: 26 mmol/l
Cholesterol oxidase: 200 U/L
Cholesterol esterase: 300 U/L
Peroxidase 1250 U/L
4-Aminoantipipipipipipine 0.4 mmol/l
Cholesterol Standard 200 mg/dL (5.17mmol/l)
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
6x65ml |
||
14 |
Urea quantitative testing reagent |
17 |
Box |
Method: UV
Measurement range: 4.8 - 400 mg/dl
Main ingredients:
R1: Tris buffer pH 7.8: 50 mmol/l
GLDH ≥ 0.80 U/L
Urease ≥ 12 U/ml
R2: Tris* buffer pH 9.6: 100 mmol/l
2-Oxoglutarate 8.3 mmol/l
NADH ≥ 0.23 mmol/l
Standard:
Urea Standard (cat.: 823s): 50 mg/dl
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 4x66ml
R2: 4x16ml |
||
15 |
GOT test reagent (AST) |
25 |
Box |
Method: ifcc
Measurement range: 3 - 1000 U/L
Detection limit: 1.5 U/L
Main ingredients:
R1: Tris buffer pH 7.8: 100 mmol/l
L-ASPARTATE: 200 mmol/l
Mdh ≥ 1 ku/l
Ldh ≥ 2 ku/l
R2: NADH ≥ 1.5 mmol/l
2-Oxoglutarate: 12 mmol/l
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 6x66ml
R2: 6x16ml |
||
16 |
GPT test reagent (ALT) |
25 |
Box |
Method: ifcc
Road measurement: 1.7 - 900 U/L
Detection limit: 4 U/L or 0.07 µkat/l
Main ingredients:
R1: Tris buffer pH 7.4: 100 mmol/l
L-alanine 500 mmol/l
LDH 1200 U/L
R2: NADH2: 0.18 mmol/l
2-Oxoglutarate: 15 mmol/l
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 6x66ml
R2: 6x16ml |
||
17 |
Glucose quantitative test reagent |
45 |
Box |
Method: God-PAP (Glucose Oxidase/ Peroxidase)
Measurement range: 0.36 - 963 mg/dl
Detection limit: 2 mg/dl
Main ingredients:
Phosphate buffer, pH 7.5: 0.1 mol/l
Phenol: 7.5 mmol/l
God: 12000 U/L
POD: 660 U/L
4-Amino-Antyrine: 0.40 mmol/l
Standard substance:
Glucose: 100 mg/dl
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
6x66ml |
||
18 |
Creatinine quantitative testing reagent |
15 |
Box |
Method: Jaffe
Ranking range: Serum/plasma: 1.0 - 2500 µmol/I
Discovery limit: 0.1mg/dl (8.8 µmol/l)
Main ingredients:
R1: Sodium hydroxide 0.2 mol/l
R2: Picric acid 25 mmol/l
Creatinine Standard: 2 mg/dl
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 4x66ml
R2: 4x16ml |
||
19 |
Calibration quality testing for biochemical testing |
25 |
Jar |
Calibrated serum is dried based on human serum, which can be used for calibration of biochemical analysts:
Total Acid Phosphatase, Non-Prostatic, Albumin, ALK. Phosphatase, ALT/GPT, α-amylase, A-Amylase Pancreatic, AST/GOT, Bilirubin Total, Bilirubin Direct, Calcium, Cholesterol Total, Cholininesterase, CK-NAC, CK-MB, Creatinine, Copper, IRON, GLUCOSE, GGT, HDL-C, LACTATE, LACTATE, LACTATE LDH-P, LDH-L, Lipase, Magnesium, Phosphate Inorganic, Protein Total, Triglycerides, Uric Acid, Urea, Zinc.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
5ml |
||
20 |
Biochemical testing materials for biochemical testing level 1 |
60 |
Jar |
Dry dried control material is based on human plasma, which has been removed fibrin for the following measurement quantities:
Total Acid Phosphatase, Non-Prostatic Phosphatase, Albumin, ALK. Phosphatase, ALT/GPT, α-amylase, A-Amylase Pancreatic, AST/GOT, Bilirubin Total, Bilirubin Direct, Calcium, Cholesterol Total, HDL-Cholesterol, LDL-CHOLesterol, Cholinesterase, CK-MB, CK-NAC, Copper, Creatinine, GGT, Iron, Iron, Iron, Iron, GGT, GGT Lactate, LDH-P, LDH-L, Lipase, Magnesium, Phosphate Inorganic, Protein Total, Triglycerides, Uric Acid, Urea, Zn.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
5ml |
||
21 |
Biochemical testing materials level 2 |
60 |
Jar |
Dry dried control material is based on human plasma, which has been removed fibrin for the following measurement quantities:
Total Acid Phosphatase, Non-Prostatic Phosphatase, Albumin, ALK. Phosphatase, ALT/GPT, α-amylase, A-Amylase Pancreatic, AST/GOT, Bilirubin Total, Bilirubin Direct, Calcium, Cholesterol, HDL-CHOLesterol, LDL-CHOLICLEROL, Cholinesterase, CK-MB, CK-NAC, Copper, Creatinine, GGT, Lactate, LDH-P, LDH-L, Lipase, Magnesium, Phosphate Inorganic, Protein Total, Triglycerides, Uric Acid, Urea, Zinc.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
5ml |
||
22 |
Qualitative and semi -quantitative test reagent Anti Streptolysin O (ASO) |
1 |
Box |
Qualitative and semi -quantitative test reagent Anti Streptolysin O (ASO)
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
100 test |
||
23 |
Alcohol Ethanol quantitative testing reagent |
3 |
Box |
Measurement range: 0-5g/l
Main wavelength 340nm; The extra wavelength 405nm.
Main ingredients:
Buffer pH 8.3 300 mmol/l
NAD+ 10 mmol/l
Alcohol dehydrogenase (ADH) ³ 200 ku/l
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
R1: 1x60ml
R2: 1x20ml |
||
24 |
ALCOHOL Ethanol Quantitative Testing |
15 |
Box |
Main ingredients:
Modined from albumin serum with additional preservatives and stabilizers.
The control ethanol contains the reaction mass of: mixture of 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-2h isothiazol-3-one (3: 1)
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
1x1ml |
||
25 |
Quality control material for quantitative test of alcohol ethanol |
30 |
Box |
Preparated from albumin serum with preservatives and stabilizers. Price:
- Control 1: ethyl alcohol: 37.0 mg/dl
- Control 2: ethyl alcohol: 95.0 mg/dl
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
2x1ml |
||
26 |
Chemicals with alkaline biochemical washing |
15 |
Can |
Main ingredients:
Alkali <10.0%
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
2L |
||
27 |
Disinfectant chemicals to wash chamber for biochemical machines |
40 |
Bottle |
Main ingredients:
Detergent <1.0%
Preservative <10.0%
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
500ml |
||
28 |
Blood -type testing reagent A |
12 |
Jar |
Single antibodies Anti A (line 11h5) |
Tien Lang Health Center |
10ml |
||
29 |
Blood -type testing reagent B |
12 |
Jar |
ANTI B series antibodies (6f9 line) |
Tien Lang Health Center |
10ml |
||
30 |
AB blood type testing reagent |
12 |
Jar |
Single antibodies A, B (line 11h5 + 6f9 + ES-15) |
Tien Lang Health Center |
10ml |
||
31 |
Blood -type testing reagent d |
10 |
Jar |
A mixture of single -class IGM and IgG (P3x61+Nath119+Lor15C9) |
Tien Lang Health Center |
10ml |
||
32 |
Chemicals for hematological analysts |
35 |
Bin |
Main ingredients:
Sodium Chloride <0.9%
Potassium Chloride <0.06%
Buffer <0.3%
Preservative <0.1%
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
20L |
||
33 |
Red blood cell solution |
50 |
Bottle |
Main ingredients:
Detergent <2.0%
Buffer <1.0%
There is a QR code that chemical management is built in.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
500ml |
||
34 |
Cleaning solution and maintenance of hematurian machine |
40 |
Bottle |
Main ingredients:
Detergent <0.5%
Sodium Chloride <1.0%
Buffer <0.3%
Preservative <0.4%
Proteolytic enzyme <2.0%
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
1L |
||
35 |
Wash chemicals for testing machines |
10 |
Jar |
Main ingredients:
Sodium hypochlorite <8.0%
Sodium hydrate <2.0%
Limit: The reagent must be used within the environmental temperature of 15-35 degrees C.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
50ml |
||
36 |
Total Protein testing reagent |
10 |
Box |
Method: Biuret
Road measurement: 0 - 15 g/dl
Detection limit: 0.2 g/dl or 2.0 g/l
Main ingredients:
Potassium iodide 30 mmol/l
Potassium sodium tartrate 32 mmol/l
Copper Sulphate 18 mmol/l
Sodium hydroxide 200 mmol/l
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
5x66ml |
||
37 |
Calibration substance for 3 component hematology tests |
25 |
Jar |
Main ingredients:
Healthy Mammal Blood (Pig), Preservatives and Cell Stabilizers.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
3ml |
||
38 |
Urine tests 11 parameters |
200 |
Box |
Main ingredients:
Ascorbic Acid: 2.6-dichloro-Phenol-Indophenol 0.5mg.
Leukocytes: Indoxoxyl ester 1.4mg; Diazonium salt 0.7mg.
Ketone: Sodium nitroprusside 30.0mg.
Nitrite: sulfanilamide 0.65mg; N- (naphthyl) -ethylenediammonium dihydrochloride 0.45mg.
Urobilinogen: Fast Blue B Salt 1.2mg.
Bilirubin: 2.4-dichlorobenzene diazonium 14.3mg.
Protein: tetrabromphenol Blue 0.36mg.
Glucose: Glucose Oxidase 6.2mg; Peroxidase 2.8mg; 4-Aminoantipipipipipine 0.08mg.
Specific Gravity: Bromthymol Blue 0.4mg; Sodium Poly Methyl Vinyl Acetate Maleic 16mg.
Blood: cumene hydroperoxide 35.2mg; 3.3 ', 5.5'-Tetramethylbenzidine 2.0mg.
pH: bromocresol green 0.2mg; Brominylenol Blue 3.3mg.
Products originating in countries G7
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
100 test |
||
39 |
Drug test 5 parameters (AMP/met/MOP/THC/KET (COC)) |
2.500 |
kiểm TRA |
- Visitors to the side chromatography to detect qualitative types of drugs, drugs and alcohol metabolites at the following levels of urine: MOP 300ng/ml; AMP 500ng/ml; Thc 50ng/ml; COD 300ng/ml; Her 10ng/ml.
- Ingredients: containing single -line antibody binding particles and drug -protein complexes. A goat antibody is used in each line.
- Sensitivity: 100%
- Specificity: 100%
- Accuracy: AMP: 99,925%; COD: 99.9%; THC: 99.92%; MOP: 99.93%; 6-MAM (Heroin): 99.9%
- Cross reaction: No cross-reaction with compounds at a concentration of 100µg/ml: acetophenetidin, n-acetylprocainamide, acetylsalicylic acid ....
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
25 Test/ Kit |
||
40 |
Test test for qualitative HCG in urine |
100 |
kiểm TRA |
- Model: urine samples.
- Performance characteristics:
+ The lowest detection limit of 10 ng/ml
+ Sensitivity: 100.00%
+ Specificity: 100.00%
+ Accuracy: 100.00%
- Testing used in combination with antibodies, including the result of a single HCG antibodies, selectively detects the increasing HCG concentration.
- The control line includes the goat's multi -line antibodies, including a single HCG antibody to detect a selective increase in HCG concentration.
- The control line includes multi -stream antibodies of goats and yellow glue particles.
- Read the results after 5 minutes.
- Store in the form of packaging in a closed bag at a temperature of 2 ° C ~ 30 ° C and the relative humidity is about 40%-60%
Quality standard ISO 13485: 2016 |
Tien Lang Health Center |
100 Test/ Box |
||
41 |
Test/tray test antibody antibody HCV |
500 |
kiểm TRA |
The tray tests for anti -anti -viral antibodies (whole / serum / serum / serum
Plasma) is a fast -tested immunity test to detect antibodies of antibodies
Hepatitis C virus in whole blood, serum or plasma of humans.
Recombinant HCV antigen (containing Core, NS3, NS4 and NS5) are fixed in the testing area on the nitrocellulose membrane.
- Public area: Recombinant antigen-2 410ng.
- Make results (t): Recombinant antigen-1 260ng
- Demonstration (C): 500ng antibodies of IgG goats
Diagnostic effect compared to the Method of HCV CMIA
Sensitivity: 100%(95%CI*: 99.4%-100%)
Specificity: 100%(95%CI*: 99.8%-100%)
Accuracy: 100%(95%CI*: 99.9%-100%)
*Reliable space
Not interfered by the following substances at the corresponding concentration
Acetaminophen: 20 mg/dl, caffeine: 20 mg/dl
Acetylsalicylic acid: 20 mg/dl, Gentisic acid: 20 mg/dl. |
Tien Lang Health Center |
40 Test/Box |
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