Duns Number:794519020
Device Description: For Collection of Plasma Product by Centrifugation. For Use With the ALYX System. Sterile For Collection of Plasma Product by Centrifugation. For Use With the ALYX System. Sterile Fluid Path.
Catalog Number
4R5730
Brand Name
ALYX Plasma Kit
Version/Model Number
4R5730
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 19, 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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
BK130030,BK130030
Product Code
GKT
Product Code Name
Separator, Automated, Blood Cell, Diagnostic
Public Device Record Key
6d84b13a-cbed-4e59-b69a-e1477129756c
Public Version Date
May 20, 2022
Public Version Number
4
DI Record Publish Date
September 08, 2016
Package DI Number
10811137012913
Quantity per Package
6
Contains DI Package
00811137012916
Package Discontinue Date
January 19, 2018
Package Status
Not in Commercial Distribution
Package Type
Carton
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8 |