Duns Number:080690327
Device Description: AXP Accessory
Catalog Number
8-5104
Brand Name
Counterweight, AXP
Version/Model Number
8-5104
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
BK070006
Product Code
OAO
Product Code Name
Cord Blood Processing System And Storage Container
Public Device Record Key
308c97a1-7360-4f0c-a09a-b49d3cad8090
Public Version Date
January 12, 2021
Public Version Number
5
DI Record Publish Date
April 05, 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 | 22 |
2 | A medical device with a moderate to high risk that requires special controls. | 26 |