FDA UDI Not in Commercial Distribution 🇺🇸 United States

TRUMATCH

DI: 10603295169352 · Model: 420697 · DEPUY ORTHOPAEDICS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRUMATCH
Primary DI
10603295169352
Version / Model
420697
Catalog Number
420697
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-03-24
Public Version
7
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
08892291-db4b-41ce-9589-7b7ffd01241f
Distribution End Date
2021-06-09

Device Description

TRUMATCH RESECTION GUIDE TIBIAL SIZE 4 RIGHT

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

GMDN Terms

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

Identifiers

Type ID
Primary 10603295169352

Customer Contacts