Multi Drug Panel Doa Test for Self Testing with FDA

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Min Order 10000 Pieces
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Shipping From Henan, China
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Henan Season Medical Device Co., Ltd.

VIP   Audited Supplier 4 years
Profile Certified by SGS/BV
SG-037
IVD Reagent
99.5%
Urine
CE FDA
Panel
Multi-Drug Test Panel
2-3 Mins
2 Years
Vitro Diagnostic Reagent
SD
Carton
Hangzhou
3822190090
Product Description
Multi Drug Panel Doa Test for Self Testing with  FDA

 
One Step Drug of Abuse Urine Test is a simple, direct binding immunoassay for rapid and qualitative detection methods. The test is based on the principle of competitive and restrains immunoassay for determination of drug of abuse (e. g AMP/MET/MOR/THC/COC/PCP/ BAR/BEN/MTD/TCA/MDMA/BUP) and its metabolites presence in urine.

Features:


Multiple Drug Tests in One Go

Fast results  

Easy visually interpretation

Simple operation, no equipment required 

High accuracy


Product Parameters:
 
PrincipleChromatographic Immunoassay 
FormatPanel 
SpecimenUrine
CertificateCE/FDA
Reading Time5 minutes
Pack 25 T
Storage  Temperature 2-30°C
Shelf Life2 Years
Cut-OffRef. Analytes

Picture Display:

TEST PROCEDURE:

Interpreting results:

Negative:Two pink-colored bands appear,one in the control region and one in the test region. A negative result indicates free drug is absent from urine or at concentrations lower than the detection cut-off level of the test.

Positive:One pink-colored band appears in the control region with no apparent band appering in the test region. A positive result indicates free drug is present in urine at concentrations at or exceeding the detection cut-off  level of the test.

Invalid:No band appears in the control region,or a pink-colored band appears in the test region only. An invalid test result may be due to improper assay procedures or damage to the device. If resultes are invalid, the assay is inconclusive and the specimen should be re-tested using a new test device.



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