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CompoMaster Net G5

FDA UDI

Class I (US FDA UDI)

by Fresenius Kabi

Identity

Trade Name
CompoMaster Net G5 FDA UDI
Generic Name
Blood component separator, automated FDA UDI
Device Name
The CompoMat G5 / CompoMaster Net G5 System is intended as an automated blood component separator used for blood component separation and preparation. FDA UDI
Model / Reference
9025571 FDA UDI
Description
The CompoMat G5 / CompoMaster Net G5 System is intended as an automated blood component separator used for blood component separation and preparation. FDA UDI

Identifiers

Catalog Number
9025571 FDA UDI
Primary DI / UDI-DI
04086000860581 FDA UDI
FDA Product Code
KSS FDA UDI
GMDN Term
Blood component separator, automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.9050 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood component separator, automated

CompoMaster Net G5 by Fresenius Kabi — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood component separator, automated.

Cleared under the same submission

BK110012 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fresenius Kabi

Sources (1)

  • FDA UDI d102c914-48e1-4bc6-9a06-4d871a080a89 36 fields · synced Jun 8, 2026