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Trigen Max 72502042

by Smith & Nephew, Inc.

Ref 72502042

Trigen Max 72502042 is a device classified as Class IIa in the EU and Class I in the US made by Smith & Nephew, Inc., registered in EUDAMED on 21 Sep 2026 (Basic UDI-DI 0885556SN000315LS) and listed in FDA GUDID since 7 May 2025 (UDI-DI 00885556896105), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0885556SN000315LS Basic UDI-DI 00885556896105UDI-DIDate21 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00885556896105 UDI-DI Date7 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0885556SN000315LS registered 21 Sep 2026 Active
  • FDA GUDID UDI-DI 00885556896105 listed 7 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00885556896105
  2. Registered EUDAMED 0885556SN000315LS

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  • Withdrawn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
Medullary canal orthopaedic reamer, rigid
Device name
Memphis Class IIA SNOI-TF-027 Reamers
Model / Ref / Catalog
72502042
Primary DI / UDI-DI
00885556896105
Basic UDI-DI
0885556SN000315LS
FDA product code
HTO
EMDN code
L091102 Orthopaedic prostheses reamers and burs, reusable
GMDN term
Medullary canal orthopaedic reamer, rigid
Device class
Class IIa EUDAMED
Class I GUDID
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Medullary canal orthopaedic reamer, rigid

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE.

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)