Duns Number:163610020
Device Description: U-UCPTM Drug Test Screen 12 Panel Drug Test CupAMP/BAR/BUP/BZO/COC/MET/MDMA/MTD/MOP/OXY/PC U-UCPTM Drug Test Screen 12 Panel Drug Test CupAMP/BAR/BUP/BZO/COC/MET/MDMA/MTD/MOP/OXY/PCP/THCwith Adulteration strip (S.G./CRE/pH)
Catalog Number
U-DUD-20124
Brand Name
U-UCPTM Drug Test Screen 12 Panel Drug Test Cup
Version/Model Number
U-DUD-20124
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
May 23, 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
4d7c5e25-b23e-4e79-8622-fb6b1f8109cc
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
May 24, 2021
Package DI Number
20817038022065
Quantity per Package
8
Contains DI Package
10817038022068
Package Discontinue Date
May 23, 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. | 2 |