FDA UDI In Commercial Distribution 🇺🇸 United States

JOURNEY

DI: 00885556692271 · Model: 74016472 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JOURNEY
Primary DI
00885556692271
Version / Model
74016472
Catalog Number
74016472
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-13
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
4e19b604-3e7f-4b9f-a172-036a3a7971cc

Device Description

17MM PIN - NON STERILE

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
66792 Intraoperative orthopaedic bone pin/screw, reusable

Identifiers

Type ID
Primary 00885556692271

Customer Contacts