Duns Number:163610020
Device Description: 10-Panel Drug Test Cup COC/THC/OPI/AMP/MET/BZO/MTD/OXY/MDMA/BUP
Catalog Number
UCC-10-1L
Brand Name
National Test Systems
Version/Model Number
UCC-10-1L
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
-
Product Code
DIO
Product Code Name
Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Public Device Record Key
83cda8d8-2bd6-4e6f-826e-81a9f1556d88
Public Version Date
June 10, 2022
Public Version Number
4
DI Record Publish Date
September 30, 2016
Package DI Number
20817038021075
Quantity per Package
8
Contains DI Package
10817038021078
Package Discontinue Date
-
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 |