FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOFIX GALAXY FIXATION SYSTEM

DI: 18052469476109 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ORTHOFIX GALAXY FIXATION SYSTEM
Primary DI
18052469476109
Version / Model
1
Catalog Number
99-94004
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-15
Public Version
1
Public Version Date
2026-04-23
Public Version Status
New
Public Device Record Key
e863f122-df18-453e-8033-2e6b48477b2e

Device Description

GALAXY FIXATION GEMINI FOOT SUPPORT KIT COMPLETE STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
67571 External orthopaedic fixation system noninvasive component, single-use

Identifiers

Type ID
Primary 18052469476109

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113770 000