ALYX Plasma Kit - For Collection of Plasma Product by - Fresenius Kabi AG

Duns Number:315654579

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.

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

4R5730

Brand Name

ALYX Plasma Kit

Version/Model Number

4R5730

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

GKT

Product Code Name

Separator, Automated, Blood Cell, Diagnostic

Device Record Status

Public Device Record Key

468d22c2-82c7-47e9-8240-8c50174488d0

Public Version Date

May 06, 2022

Public Version Number

1

DI Record Publish Date

April 28, 2022

Additional Identifiers

Package DI Number

14086000101025

Quantity per Package

6

Contains DI Package

04086000101028

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton

"FRESENIUS KABI AG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 5
2 A medical device with a moderate to high risk that requires special controls. 87
U Unclassified 2