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Affinity®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
AFFINITY® FDA UDI
Generic Name
Cardiopulmonary bypass system filter, arterial blood line FDA UDI
Device Name
FILTER 61399409434 AFFINITY 6CA ARFIL20M FDA UDI
Model / Reference
61399409434 FDA UDI
Description
FILTER 61399409434 AFFINITY 6CA ARFIL20M FDA UDI

Identifiers

Primary DI / UDI-DI
00613994094346 FDA UDI
510(k) Number
K994208 FDA UDI
FDA Product Code
DTM FDA UDI
GMDN Term
Cardiopulmonary bypass system filter, arterial blood line FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4260 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Pore Size — 20.0 Micrometer FDA UDI

Category: Cardiopulmonary bypass system filter, arterial blood line

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

Similar devices

Also classified as Cardiopulmonary bypass system filter, arterial blood line.

Cleared under the same submission

K994208 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 dc6ff15a-b898-41e7-be61-a8fbc5bbefbf 37 fields · synced May 30, 2026