• in Vitro Diagnostic One Step Syphilis Blood Test Strip
  • in Vitro Diagnostic One Step Syphilis Blood Test Strip
  • in Vitro Diagnostic One Step Syphilis Blood Test Strip
  • in Vitro Diagnostic One Step Syphilis Blood Test Strip
  • in Vitro Diagnostic One Step Syphilis Blood Test Strip
  • in Vitro Diagnostic One Step Syphilis Blood Test Strip

in Vitro Diagnostic One Step Syphilis Blood Test Strip

Type: Test Strips & Test Tube
Material: Non-woven Fabric
Ethylene Oxide Sterilization: Ethylene Oxide Sterilization
Quality Guarantee Period: Two Years
Logo Printing: With Logo Printing
Transport Package: 1PCS/Foil Pouch, 40 PCS/Valve Bag, 2000 PCS/Carton
Samples:
US$ 0/Piece 1 Piece(Min.Order)
| Request Sample
Customization:

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Basic Info.

Model NO.
AMC22318
Specification
Strip: 2.5, 3.0; Cassette: 3.0, 4.0
Trademark
Medipharm, OEM
Origin
China
HS Code
90183900
Production Capacity
100000ctns /Month

Product Description

 
 

Product Description

in Vitro Diagnostic One Step Syphilis Blood Test Strip 

(TP) Syphili Rapid Test Kit

Function

Rapid test for Infectious disease

Format

Strip/cassette

Specimen

serum/plasma/whole blood

Sensitivity

Over 99%

Accuracy

Over 99%

Valid

Room temperature: 24months

Buffer

Available (whole blood)

TEST PROCEDURE

1.  To begin testing; open the sealed pouch by tearing along the notch.. Remove the test form the pouch.

2.lay the cassette flat on a clean, dry, nonabsorbent surface ,draw about 30ul whole blood into the sample pad.

3.Then draw one drop of Sodium Chloride(about 20ul)into the sample well as well.

4.Wait for colored bands to appear.Read results within 15 minutes. Do not read results after 20 minutes

INTERPRETATION OF RESULTS

Negative: Only one pink band appears on test region of the Cassette. This indicates that there is no detectable anti-TP in the whole blood.

Positive: Two pink bands appear on test region of the Cassette. This indicates that the specimen contains detectable amount of anti-TP.

Invalid: If without colored band appears on test region, this is an indication of a possible error in performing the test. The test should be repeated using a new device.

 
   

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