Duns Number:463625602
Device Description: The DG Gel 8 ABO/Rh card is for the determination of ABO forward and reverse group and D a The DG Gel 8 ABO/Rh card is for the determination of ABO forward and reverse group and D antigen on the surface of red blood cells, and for ABO Compatibility Test in human blood samples.For use with Manual Method. Not for use with Erytra or WADiana Compact.For in vitro diagnostic use.
Catalog Number
210118
Brand Name
DG Gel 8 ABO/Rh
Version/Model Number
210118
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 31, 2021
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
-
Product Code
-
Product Code Name
-
Public Device Record Key
b2173fec-693d-4b4b-b17b-25fbc2683554
Public Version Date
November 17, 2021
Public Version Number
4
DI Record Publish Date
October 29, 2015
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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 9 |