Duns Number:421302978
Device Description: 12P DRUG TEST DIPCARD
Catalog Number
-
Brand Name
co-innovation
Version/Model Number
12P DIPCARD
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 15, 2018
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
K153050,K153050,K153050,K153050
Product Code
DIO
Product Code Name
Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Public Device Record Key
2cb61094-3f6a-4b0f-8ba5-a0982b28672f
Public Version Date
June 10, 2022
Public Version Number
4
DI Record Publish Date
June 08, 2018
Package DI Number
36970429841261
Quantity per Package
10
Contains DI Package
26970429841264
Package Discontinue Date
June 08, 2018
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 10 |