FDA UDI In Commercial Distribution 🇺🇸 United States

GALAXY FIXATION GEMINI

DI: 18052469472583 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GALAXY FIXATION GEMINI
Primary DI
18052469472583
Version / Model
1
Catalog Number
194500
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-27
Public Version
1
Public Version Date
2022-01-04
Public Version Status
New
Public Device Record Key
dc8c85fa-f299-4198-8648-10b685608b5e

Device Description

GALAXY FIXATION GEMINI SCREW GUIDE

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
No
MRI Safety
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
47457 Orthopaedic trocar blade, reusable

Identifiers

Type ID
Primary 18052469472583

Customer Contacts