FDA UDI In Commercial Distribution 🇺🇸 United States

Journey II

DI: 00885556781852 · Model: E0016949-1 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Journey II
Primary DI
00885556781852
Version / Model
E0016949-1
Catalog Number
E0016949-1
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-16
Public Version
2
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
3ad81f48-5f4e-435a-a6ba-a2f0ad07d4f4

Device Description

JOURNEY SHIFT BLOCK

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00885556781852

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K121393 000