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Trigen Max 72501008

by Smith & Nephew, Inc.

Ref 72501008

Trigen Max 72501008 is a Class I device made by Smith & Nephew, Inc., registered in EUDAMED on 9 Sep 2026 (Basic UDI-DI 0885556SN000141LH) and listed in FDA GUDID since 7 May 2025 (UDI-DI 00885556895702), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0885556SN000141LH Basic UDI-DI 00885556895702UDI-DIDate9 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00885556895702 UDI-DI Date7 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0885556SN000141LH registered 9 Sep 2026 Active
  • FDA GUDID UDI-DI 00885556895702 listed 7 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00885556895702
  2. Registered EUDAMED 0885556SN000141LH

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  • Withdrawn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
Instrument tray, reusable
Device name
Memphis Class I SNOI-TF-030 Trays
Model / Ref / Catalog
72501008
Primary DI / UDI-DI
00885556895702
Basic UDI-DI
0885556SN000141LH
FDA product code
OJH
EMDN code
V0402 Clinical use trays and bowls
GMDN term
Instrument tray, reusable
Device class
Class I
Regulation number
878.4800
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: Instrument tray, reusable

Similar devices in this category

Other devices filed under CLINICAL USE TRAYS AND BOWLS.

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)