 The RDS InCup is an all-inclusive test cup for the simultaneous detection of up to 12 drugs of abuse in a urine specimen. The InCup incorporates collection and testing in one device, in just one step. Once the donor provides the specimen, the results are revealed in minutes without any manipulation of the specimen or the test. InCup is available in many standard configurations, with custom drug test configurations also available upon request.
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For more information or to place an order:
Contact a Sales Representative
Email a Customer Service Representative
Or to speak with a customer service representative, call:
1-800-227-1243
ext. 2
Product Information and Training
RDS InCup
Product Brochure
(PDF)
RDS InCup
Quick Reference Guide
(PDF)
Online Product Training
Technical Support
For 24/7/365
support call
1-800-227-1243
ext. 3
or email ABMC
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AMP
Amphetamines 1000 ng/ml
BAR
Barbiturates 300 ng/ml
BZO
Benzodiazepines
300 ng/ml
BUP
Buprenorphine 12.5 ng/ml
COC
Cocaine 150 or 300 ng/ml
MDMA
Ecstasy 1000 ng/ml
MTD
Methadone 300 ng/ml
METH
Methamphetamines
1000 ng/ml
NIC*
Nicotine 200 ng/ml
OPI
Opiates 300 or 2000 ng/ml
OXY
Oxycodone 100 ng/ml
PCP
Phencyclidine 25 ng/ml
PPX
Propoxyphene 300 ng/ml
THC
Marijuana 50 ng/ml
TCA
Tricyclic 1000 ng/ml
Antidepressants
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Integrated collection and testing
Temperature strip on cup
Clear collection: visual integrity check
Collect sample, read results in 3-5 minutes
No timing required: control line indicator
Closed specimen cup: limits exposure
Ship in same container for confirmation
Test 2-12 drugs per test
Customized configurations available
Multiple cut-offs
Specimen Validity Test built in (optional)
Tamper preventive security seal available
Each test has built-in procedural control
Results stable for up to one hour
>99% correlation to GC/MS at 95% confidence level
Colloidal gold technology
Tested for cross-reactivity against over 600 compounds
SAMHSA cut-off levels
Integrated test strips are US FDA 510(k) cleared
Web based training with certification
Onsite training
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* Assay is not US FDA 510(k) cleared
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