Skip to content

Trumatch 420582

by Depuy Orthopaedics, Inc.

Ref 420582

Trumatch 420582 is a device classified as Class IIa in the EU and Class III in the US made by Depuy Orthopaedics, Inc., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-USMF000038159000275YL) and listed in FDA GUDID since 22 Feb 2019 (UDI-DI D-USMF000038159000275YL), active as of 7 Nov 2026.

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

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-USMF000038159000275YL Basic UDI-DI D-USMF000038159000275YLUDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-USMF000038159000275YL UDI-DI Date22 Feb 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-USMF000038159000275YL registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI D-USMF000038159000275YL listed 22 Feb 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D-USMF000038159000275YL
  2. Registered EUDAMED B-USMF000038159000275YL

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Trumatch
Generic name
Orthopaedic prosthesis implantation positioning instrument, single-use
Model / Ref / Catalog
420582
Primary DI / UDI-DI
D-USMF000038159000275YL EUDAMED
10603295430780 GUDID
Basic UDI-DI
B-USMF000038159000275YL
FDA product code
NJL, JWH, OOG
EMDN code
P091399 Orthopaedic implant instruments, single-use - other
GMDN term
Orthopaedic prosthesis implantation positioning instrument, single-use
Device class
Class IIa EUDAMED
Class III GUDID
Regulation number
888.3560
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D-USMF000038159000275YL
GUDID
10603295430780
Device classEUDAMED
Class IIa
GUDID
Class III

The registries describe this device under different primary UDI-DIs (EUDAMED lists D-USMF000038159000275YL; FDA GUDID lists 10603295430780), so their flags are not compared. Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class III in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Orthopaedic prosthesis implantation positioning instrument, single-use

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Depuy Orthopaedics, Inc.

See all devices from Depuy Orthopaedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)