Skip to content

Depuy Orthopaedic Instruments

by DePuy Ireland UC 18 variants

Ref 2447-26-000, 2178-70-100Model TruMatch Instrument Case/Tray

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0603295a0054799 Basic UDI-DI Date30 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10603295124818 UDI-DI Date24 Sep 2018ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
Depuy Orthopaedic Instruments EUDAMED
Depuy EUDAMEDGUDID
Generic Name
Instrument tray, reusable
Fluted surgical drill bit, reusable
Device Name
Drill
Instrument Case/Tray
Model / Ref / Catalog
2447-26-000, 2178-70-100, TruMatch Instrument Case/Tray, 217870100, 244726000
Primary DI / UDI-DI
10603295124818, 10603295096757
Basic UDI-DI
0603295a0054799, 0603295a000107R
Direct Marketing DI
10603295124818
10603295096757
FDA Product Code
FSM, HTW
EMDN Code
L091102, L0999
GMDN Term
Instrument tray, reusable
Fluted surgical drill bit, reusable
Device Class
Class IIa EUDAMED
Class I EUDAMEDGUDID
Regulation Number
878.4800, 888.4540
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
Class I
GUDID
Class I

Manufacturer details

EUDAMED SRN
IE-MF-000007377

Related devices

Category: Acetabular orthopaedic reamer

Other devices from DePuy Ireland UC

See all devices from DePuy Ireland UC →

Properties

  • CMR Substance YesEUDAMEDNoEUDAMED
  • Premarket Exempt
  • Lot / Batch Number

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No