Duns Number:174517060
Device Description: QuikStrip Multidrug 5 Test, AMP 500, COC 300, MET 500, OP I 2000, THC 50
Catalog Number
-
Brand Name
QuikStrip Multidrug Screening Dip Card Test
Version/Model Number
30500
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)
-
Over the Counter (OTC)
-
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
b4545dd6-0da8-4670-9d69-00b19e472277
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
June 05, 2017
Package DI Number
20748349000377
Quantity per Package
4
Contains DI Package
10748349000370
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Shipper Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 28 |