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Trillium® Affinity Nt®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
TRILLIUM® AFFINITY NT® FDA UDI
Generic Name
Extracorporeal membrane oxygenator FDA UDI
Device Name
OXYGENATOR 95250 AFFINITY 2PK 511T 541TT FDA UDI
Model / Reference
95250 FDA UDI
Description
OXYGENATOR 95250 AFFINITY 2PK 511T 541TT FDA UDI

Identifiers

Primary DI / UDI-DI
00721902648892 FDA UDI
510(k) Number
K191029 FDA UDI
K973760 FDA UDI
FDA Product Code
DTZ FDA UDI
JOW FDA UDI
GMDN Term
Extracorporeal membrane oxygenator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4350 FDA UDI
870.5800 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

Category: Extracorporeal membrane oxygenator

Trillium® Affinity Nt® 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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 7b4873bf-d086-4daa-a395-4b776882d7e4 36 fields · synced May 30, 2026