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Trumatch

FDA UDI

Class III (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
TRUMATCH FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, single-use FDA UDI
Device Name
TRUMATCH PERSONALIZED SOLUTIONS PIN GUIDE FEMUR - CT KNEE FOR USE WITH: LEFT FDA UDI
Model / Reference
420580 FDA UDI
Description
TRUMATCH PERSONALIZED SOLUTIONS PIN GUIDE FEMUR - CT KNEE FOR USE WITH: LEFT FDA UDI

Identifiers

Catalog Number
420580 FDA UDI
Primary DI / UDI-DI
10603295430810 FDA UDI
FDA Product Code
NJL FDA UDI
JWH FDA UDI
OOG FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, single-use FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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: Orthopaedic prosthesis implantation positioning instrument, single-use

Trumatch by Depuy Orthopaedics, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Orthopaedics, Inc.

Sources (1)

  • FDA UDI d1dfc728-f241-4f40-8de1-7b6d0c5222dd 35 fields · synced Jun 8, 2026