FDA UDI In Commercial Distribution 🇺🇸 United States

OTHER EXTERNAL FIXATION

DI: 03596010591708 · Model: 71050023 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OTHER EXTERNAL FIXATION
Primary DI
03596010591708
Version / Model
71050023
Catalog Number
71050023
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-25
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
4e9a137f-ccb8-45af-a336-614ad3d8e384

Device Description

200MM X 50MM CANNULATED HALF PIN

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
48011 External orthopaedic fixation system, single-use

Identifiers

Type ID
Primary 03596010591708

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K920024 000