FDA UDI In Commercial Distribution 🇺🇸 United States

TRUMATCH

DI: 10603295384816 · Model: 42-0906 · DEPUY ORTHOPAEDICS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRUMATCH
Primary DI
10603295384816
Version / Model
42-0906
Catalog Number
420906
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
0f0c7935-ad53-458d-a43f-21b0738e7c2a

Device Description

TruMatch PERSONALIZED SOLUTIONS FEMUR RESECTION GUIDE TIBIA PIN GUIDE SET - CT KNEE FOR USE WITH: LEFT HYBRID

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OOG Knee arthroplasty implantation system
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
NJL Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 10603295384816

Customer Contacts