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Affinity Fusion®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Affinity Fusion® FDA UDI
Generic Name
Extracorporeal membrane oxygenator FDA UDI
Device Name
OXY/CVR COMBO BB841 FUSION W/BALANCE FDA UDI
Model / Reference
BB841 FDA UDI
Description
OXY/CVR COMBO BB841 FUSION W/BALANCE FDA UDI

Identifiers

Primary DI / UDI-DI
00643169354869 FDA UDI
510(k) Number
K132972 FDA UDI
FDA Product Code
DTN FDA UDI
GMDN Term
Extracorporeal membrane oxygenator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Extracorporeal membrane oxygenator

Affinity Fusion® by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extracorporeal membrane oxygenator.

Cleared under the same submission

K132972 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI bb7cdcb2-9604-4ef7-acd1-ba70f0014e39 36 fields · synced May 31, 2026