FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 03596010170910 · Model: 71021024 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
03596010170910
Version / Model
71021024
Catalog Number
71021024
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
8
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
42088fed-78a7-4ff2-8ff5-d98e5d2ad3ad

Device Description

TITANIUM HALF PIN 6MM X 30MM

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
MR Conditional
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
LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

GMDN Terms

Code Name
32854 Orthopaedic bone pin, non-bioabsorbable

Identifiers

Type ID
Primary 03596010170910

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201253 000
K953397 000