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Trigen Max 72502023

by Smith & Nephew, Inc.

Part of a family of 11 devices: see the family page

Ref 72502023

Trigen Max 72502023 is a Class I device made by Smith & Nephew, Inc., registered in EUDAMED on 21 Sep 2026 (Basic UDI-DI 0885556SN000357MA) and listed in FDA GUDID since 7 May 2025 (UDI-DI 00885556895931), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0885556SN000357MA Basic UDI-DI 00885556895931UDI-DIDate21 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00885556895931 UDI-DI Date7 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0885556SN000357MA registered 21 Sep 2026 Active
  • FDA GUDID UDI-DI 00885556895931 listed 7 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00885556895931
  2. Registered EUDAMED 0885556SN000357MA

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Trigen Max
Generic name
Orthopaedic implantation sleeve, reusable
Device name
Memphis Class IR SNOI-TF-026 L091199
Model / Ref / Catalog
72502023
Primary DI / UDI-DI
00885556895931
Basic UDI-DI
0885556SN000357MA
FDA product code
HXX
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN term
Orthopaedic implantation sleeve, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implantation sleeve, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)