Duns Number:064177324
Device Description: "Identify® Diagnostics Drug Test Cups12-Panel Drug Screening Test Cup AMP/BAR/BUP/BZO/COC/ "Identify® Diagnostics Drug Test Cups12-Panel Drug Screening Test Cup AMP/BAR/BUP/BZO/COC/MTD/MDMA/MET/MOP/OXY/PCP/THCwith Adulteration strip (S.G./CRE/pH) "
Catalog Number
ID-CP12-BUP-ADULT-AZ10
Brand Name
Identify®Diagnostics Drug Test Cups
Version/Model Number
ID-CP12-BUP-ADULT-AZ10
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
June 21, 2030
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K131811,K131811,K131811
Product Code
DIO
Product Code Name
Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Public Device Record Key
0f9f49ac-d64a-4072-8f06-faef292aad4a
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
June 21, 2019
Package DI Number
20850721007987
Quantity per Package
20
Contains DI Package
10850721007980
Package Discontinue Date
June 21, 2030
Package Status
In Commercial Distribution
Package Type
case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 8 |