Aurora Xi Plasmapheresis System - For collection of plasma by membrane - Fresenius Kabi AG

Duns Number:315654579

Device Description: For collection of plasma by membrane filtration.For Use With the Plasmacell Xi Disposable For collection of plasma by membrane filtration.For Use With the Plasmacell Xi Disposable Sets.

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More Product Details

Catalog Number

6R4612

Brand Name

Aurora Xi Plasmapheresis System

Version/Model Number

6R4612

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

-

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

BK160028,BK170057

Product Code Details

Product Code

GKT

Product Code Name

Separator, Automated, Blood Cell, Diagnostic

Device Record Status

Public Device Record Key

7a4ce3bf-522a-4599-8d96-0129558b469b

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

March 02, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"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