Aurora Plasmapheresis System Software Version 2.1

GUDID 00810020440003

Aurora Plasmapheresis System Software Version 2.1

Fresenius Kabi AG

Apheresis system
Primary Device ID00810020440003
NIH Device Record Keyfe91b685-b504-4d1f-9063-f6cfda7355e1
Commercial Distribution StatusIn Commercial Distribution
Brand NameAurora Plasmapheresis System Software Version 2.1
Version Model NumberSW 2.1
Company DUNS315654579
Company NameFresenius Kabi AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810020440003 [Primary]
GS110810020440000 [Package]
Package: [3 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GKTSeparator, Automated, Blood Cell, Diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-04
Device Publish Date2019-10-25

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