FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 03596010083012 · Model: 128120 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
03596010083012
Version / Model
128120
Catalog Number
128120
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
2025-07-14
Public Version Status
Update
Public Device Record Key
a82bb8ab-acd8-4e5a-9deb-ed260b2a2755

Device Description

STEINMANN PIN DIAMOND POINT ROUND END 9/64 X 9

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
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
HTY PIN, FIXATION, SMOOTH

GMDN Terms

Code Name
32854 Orthopaedic bone pin, non-bioabsorbable

Identifiers

Type ID
Package 23596010083016
Primary 03596010083012

Customer Contacts