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ALYX Component Collection System

FDA UDI

Class II (US FDA UDI)

by Fresenius Kabi

Identity

Trade Name
ALYX Component Collection System FDA UDI
Generic Name
Apheresis system FDA UDI
Device Name
Intended for use in blood collection establishments to collect and separate whole blood into its components. FDA UDI
Model / Reference
6R5725 FDA UDI
Description
Intended for use in blood collection establishments to collect and separate whole blood into its components. FDA UDI

Identifiers

Catalog Number
6R5725 FDA UDI
Primary DI / UDI-DI
04086000100212 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Apheresis system

ALYX Component Collection System 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

BK130030 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 34600ecc-0497-4fd9-b490-3873d9d3ef0b 35 fields · synced May 30, 2026