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TRILLIUM® Affinity® 351T

by Medtronic, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00721902363597 UDI-DI Date17 Aug 2015ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
TRILLIUM® Affinity®
Generic Name
Cardiopulmonary bypass system filter, arterial blood line
Model / Reference
351T
Primary DI / UDI-DI
00721902363597
510(k) Number
FDA Product Code
DTM
GMDN Term
Cardiopulmonary bypass system filter, arterial blood line
Device Class
Class II
Regulation Number
870.4260
GUDID distribution status
Not in Commercial Distribution
Size
Pore Size — 38.0 Micrometer

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (10)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No