Duns Number:421302978
Device Description: 17P Drug Test
Catalog Number
-
Brand Name
co-innovation
Version/Model Number
17P Drug Test
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 17, 2022
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K153050,K153050,K153050,K153050
Product Code
DIC
Product Code Name
Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method
Public Device Record Key
c853194b-3468-46d3-ad0a-82ac32987757
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
January 15, 2022
Package DI Number
16970429841700
Quantity per Package
25
Contains DI Package
06970429841703
Package Discontinue Date
January 17, 2022
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 |