FDA UDI In Commercial Distribution 🇺🇸 United States

INTRAUMA SURGICAL INSTRUMENT

DI: 08056693027956 · Model: S213 · INTRAUMA SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTRAUMA SURGICAL INSTRUMENT
Primary DI
08056693027956
Version / Model
S213
Catalog Number
S213
Company Name
INTRAUMA SPA
Labeler DUNS
387588051
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-27
Public Version
1
Public Version Date
2025-12-05
Public Version Status
New
Public Device Record Key
fc677a11-fe6c-4cc2-9f68-996a76bc0fa7

Device Description

Ø1,2mm K-Wire Sleeve

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
Yes
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
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Primary 08056693027956