Duns Number:606034197
Device Description: For Use with PakAuto
Catalog Number
403594
Brand Name
PNPP Substrate
Version/Model Number
403594
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 01, 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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
BK960059
Product Code
MYP
Product Code Name
Test,Platelet Antibody
Public Device Record Key
b1dfc5a3-885a-4669-b141-0890e24162f8
Public Version Date
August 01, 2018
Public Version Number
4
DI Record Publish Date
July 07, 2016
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. | 54 |
U | Unclassified | 36 |