FDA UDI In Commercial Distribution 🇺🇸 United States

WRISTAR MULTIAX

DI: 08056693028137 · Model: T120.903X · INTRAUMA SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
WRISTAR MULTIAX
Primary DI
08056693028137
Version / Model
T120.903X
Catalog Number
T120.903X
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
b3432805-a1d9-43b7-b3ca-bb5fdd588de2

Device Description

Trial Plates for WRISTAR MultiAx Volar Radius

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRS Plate, Fixation, Bone

GMDN Terms

Code Name
58804 Surgical implant template, single-use

Identifiers

Type ID
Primary 08056693028137

Premarket Submissions

Submission Number Supplement Number
K252959 000