FDA UDI In Commercial Distribution 🇺🇸 United States

Aurora Software Version 2.1C Upgrade

DI: 00810020440300 · Model: Version 2.1C · Fresenius Kabi AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Aurora Software Version 2.1C Upgrade
Primary DI
00810020440300
Version / Model
Version 2.1C
Catalog Number
X6S4021USB
Company Name
Fresenius Kabi AG
Labeler DUNS
315654579
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-09
Public Version
1
Public Version Date
2021-06-17
Public Version Status
New
Public Device Record Key
ddb48358-d4b5-44b0-9e3f-672bb175f07c

Device Description

AURORA Software Version 2.1C for collection of plasma by membrane filtration.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GKT Separator, Automated, Blood Cell, Diagnostic

GMDN Terms

Code Name
16405 Apheresis system

Identifiers

Type ID
Primary 00810020440300
Package 10810020440307

Premarket Submissions

Submission Number Supplement Number
BK190368 0