Duns Number:031433133
Device Description: CLIA-waived NexScreen Cup 12AMP1000/BAR300/BZO300/COC300/MDMA500/MET1000/MTD300/OPI300/OXY CLIA-waived NexScreen Cup 12AMP1000/BAR300/BZO300/COC300/MDMA500/MET1000/MTD300/OPI300/OXY100/PCP25/TCA1000/THC50
Catalog Number
NXS-61203N
Brand Name
NexScreen Cup
Version/Model Number
NXS-61203N
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"
-
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
daf3fdca-45ca-45b4-beb6-792610fbe80b
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
August 30, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 34 |