FDA UDI In Commercial Distribution 🇺🇸 United States

JOURNEY

DI: 00885556786291 · Model: 74021343 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JOURNEY
Primary DI
00885556786291
Version / Model
74021343
Catalog Number
74021343
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-19
Public Version
2
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
9a37f833-0396-4ef5-b855-43d5b56d6435

Device Description

JOURNEY II ARTICULAR STABILIZED XLPE ARTICULAR INSERT SIZE 3-4 RIGHT 11MM

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
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
33580 Uncoated knee tibia prosthesis, polyethylene

Identifiers

Type ID
Primary 00885556786291

Customer Contacts