Instant-View Cocaine Drug Test
As Low As .81 each
The Cocaine Rapid Drug Test Cassette (case of 25) is CLIA Waived & FDA 510K #K063545, simply dip the card in urine and read results in 4 minutes. - The Instant-View® Cocaine urine drug test is (simply dip & read at 4 minutes), a rapid, lateral flow diagnostic test intended to evaluate the usage of cocaine by detecting benzoylecgonine, a metabolite of cocaine, in human urine at a cut-off level of 300 ng/ml. Cocaine is a nervous system stimulant that may appear in the urine for only a few hours after use; therefore, the Instant-View® Cocaine urine drug test is designed to detect benzoylecgonine, a hydrolytic degradation product of cocaine, which may be detectable in urine for over two days after the use of cocaine. The test is for healthcare professional use only and provides only a qualitative screening test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. The test is available in cassette and dip strip formats, with the option of being included in the Instant-View® multi-drug screen test.
Cocaine urine cassette and dip strip test
Method
Lateral flow test
Cut-off level
300 ng/ml
Accuracy
> 97.8%
Precision
cassette: 93.30%
dip strip: 94.20%
Sample
Urine
Read time
4-7 minutes
Storage
Room temperature
Shelf life
24 months from date of manufacture
CLIA Classification
Waived
Feature
Benefit
Simple, one-step procedure
Fast results; minimizes user error
24-month shelf life at room temp. (from date of manufacture)
No special storage requirements to maintain stability
Small sample volume required
Tests can be reliably performed with minimal amount of specimen
Offered in cassette or dip strip format
Different formats for applying specimen
300 ng/ml cut-off level
Meets SAMHSA standards for substance abuse screening
Assigned CPT Codes
Multiple Classes: 80100QW
Single Class: 80101QW
Accepted by Medicare for reimbursement
Made in U.S.A.
Dependable, on-time supply & ready technical support
-Catalog #: 03-3052
-Quantity: 25 Tests
-FDA 510k & CLIA Waived
