FDA UDI In Commercial Distribution 🇺🇸 United States

JOURNEY

DI: 03596010558626 · Model: 74033265 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JOURNEY
Primary DI
03596010558626
Version / Model
74033265
Catalog Number
74033265
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
2944102f-da4b-4a1f-bfad-44d1cebf3d3e

Device Description

JOURNEY ARTICULAR INSERT TRIAL BCS STANDARD 5-6 LEFT 15M

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
58716 Knee tibia prosthesis trial, reusable

Identifiers

Type ID
Primary 03596010558626

Customer Contacts