Duns Number:312576506
Device Description: Blood Grouping Reagent; Gel card for use with IH-system; Card for ABO/RhD (DVI+) antigen Blood Grouping Reagent; Gel card for use with IH-system; Card for ABO/RhD (DVI+) antigen typing and direct antiglobulin test; 12 cards of 6 microtubes
Catalog Number
813130100
Brand Name
IH-Card ABO/RhD(DVI+)
Version/Model Number
813130100
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)
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
519a2041-8642-4ce0-9485-8427165789ca
Public Version Date
October 19, 2021
Public Version Number
3
DI Record Publish Date
January 20, 2017
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 | 4 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 38 |
| U | Unclassified | 21 |