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Aurora Plasmapheresis System Software Version 2.1

FDA UDI

Class II (US FDA UDI)

by Fresenius Kabi

Identity

Trade Name
Aurora Plasmapheresis System Software Version 2.1 FDA UDI
Generic Name
Apheresis system FDA UDI
Device Name
Aurora Plasmapheresis System Software Version 2.1 FDA UDI
Model / Reference
SW 2.1 FDA UDI
Description
Aurora Plasmapheresis System Software Version 2.1 FDA UDI

Identifiers

Primary DI / UDI-DI
00810020440003 FDA UDI
FDA Product Code
GKT FDA UDI
GMDN Term
Apheresis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9245 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Apheresis system

Aurora Plasmapheresis System Software Version 2.1 by Fresenius Kabi — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Apheresis system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fresenius Kabi

Sources (1)

  • FDA UDI fe91b685-b504-4d1f-9063-f6cfda7355e1 34 fields · synced Jun 1, 2026