Skip to content

Lps

by DePuy Ireland UC 90 variants

Ref 2987-22-223, 2987-99-024, 2987-22-018, 2987-22-021, 2987-99-042, 2987-70-165, 2987-72-045, 2987-99-012, 2987-99-034, 2987-72-010, 2987-22-331, 2987-40-040, 2987-22-123, 2987-72-020, 2987-22-012, 2987-70-210, 2987-99-032, 2987-70-100, 2987-40-035, 2987-25-110, 2987-72-040, 2987-22-023Model TruMatch Instrument Case/Tray, SPECIALIST 2 REAMER

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0603295a001848T Basic UDI-DI Date30 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10603295158424 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  • Withdrawn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

Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable
Knee tibia prosthesis trial, reusable
Instrument tray, reusable
Medullary canal orthopaedic reamer, rigid
Knee femur prosthesis trial, reusable
Surgical instrument handle, non-torque-limiting
Orthopaedic implant/instrument assembling device
Orthopaedic implant-instrument extension adaptor, reusable
Device Name
Instrument Case/Tray
Reamer
Inserter/Extractor
Assembly Instrument
Implant to Trial Adapter
Femoral Stem Trial
Instrument Handle C-I
Model / Ref / Catalog
2987-22-223, 2987-72-045, 2987-22-012, 2987-22-023, 2987-99-034, 2987-70-210, 2987-25-110, 2987-22-018, 2987-72-040, 2987-99-032, 2987-72-020, 2987-40-040, 2987-70-100, 2987-40-035, 2987-22-331, 2987-72-010, 2987-99-012, 2987-22-021, 2987-22-123, 2987-99-024, 2987-99-042, 2987-70-165, TruMatch Instrument Case/Tray, SPECIALIST 2 REAMER, 298772045, 298722012, 298722023, 298799034, 298770210, 298725110, 298722018, 298772040, 298799032, 298772020, 298740040, 298770100, 298740035, 298722331, 298772010, 298799012, 298722021, 298722123, 298799024, 298799042, 298770165, 298722223
Primary DI / UDI-DI
10603295158424, 10603295159162, 10603295158226, 10603295158271, 10603295159582, 10603295159063, 10603295158561, 10603295158257, 10603295159155, 10603295159575, 10603295159117, 10603295158752, 10603295158844, 10603295158745, 10603295158547, 10603295159094, 10603295159414, 10603295158264, 10603295158332, 10603295159537, 10603295159612, 10603295158974
Basic UDI-DI
0603295a001848T, 0603295a000107R, 0603295a0000886, 0603295a000458C, 0603295a000307X, 0603295a0020182, 0603295a002007Y, 0603295a0004388
Direct Marketing DI
10603295158424
10603295159537
10603295158257
10603295158264
10603295159612
10603295158974
10603295159162
10603295159414
10603295159582
10603295159094
10603295158547
10603295158752
10603295158332
10603295159117
10603295158226
10603295159063
10603295159575
10603295158844
10603295158745
10603295158561
10603295159155
10603295158271
FDA Product Code
HWB, HWT, FSM, HTO, FZY, LXH
EMDN Code
L091199, L0999, L091102
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable
Knee tibia prosthesis trial, reusable
Instrument tray, reusable
Medullary canal orthopaedic reamer, rigid
Knee femur prosthesis trial, reusable
Surgical instrument handle, non-torque-limiting
Orthopaedic implant/instrument assembling device
Orthopaedic implant-instrument extension adaptor, reusable
Device Class
Class IIa EUDAMED
Class I EUDAMEDGUDID
Regulation Number
888.4540, 888.4800, 878.4800
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

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