← Back to catalogue

Cut Guide

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 420917Model Trumatch CT Cut Guide

by DePuy Ireland UC

Identity

Trade Name
TRUMATCH FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, single-use FDA UDI
Device Name
Cut Guide EUDAMED
TRUMATCH PERSONALIZED SOLUTIONS RESECTION GUIDE FEMUR - CT KNEE FOR USE WITH: LEFT FDA UDI
Model / Reference
Trumatch CT Cut Guide EUDAMED
420917 EUDAMEDFDA UDI
Description
TRUMATCH PERSONALIZED SOLUTIONS RESECTION GUIDE FEMUR - CT KNEE FOR USE WITH: LEFT FDA UDI

Identifiers

Catalog Number
420917 FDA UDI
Primary DI / UDI-DI
10603295384878 EUDAMEDFDA UDI
Basic UDI-DI
0603295a0056193 EUDAMED
FDA Product Code
NJL FDA UDI
OOG FDA UDI
JWH FDA UDI
EMDN Code
P091399 ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class III FDA UDI
Regulation Number
888.3560 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Joint prosthesis implantation kit, single-use

Cut Guide by DePuy Ireland UC — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
DePuy Ireland UC
EUDAMED SRN
IE-MF-000007377

Sources (2)

  • EUDAMED 68adf7ef-e6d2-4193-9aa9-50e4c8608e31 61 fields · synced Aug 4, 2026
  • FDA UDI 46c44162-5710-4484-87e0-4a7f23b5348e 35 fields · synced May 30, 2026