FDA UDI In Commercial Distribution 🇺🇸 United States

Galaxy Fixation System

DI: 18033509859892 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Galaxy Fixation System
Primary DI
18033509859892
Version / Model
1
Catalog Number
99-93080
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
c5d074a4-cfc4-4f3d-a98b-4a83b4d3290f

Device Description

TRANSFIX PIN 80 MM STERILE

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
No
Has Serial Number
Yes
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
32854 Orthopaedic bone pin, non-bioabsorbable

Identifiers

Type ID
Primary 18033509859892

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113770 000

Device Sizes

Type Value Unit Text
Length 80 Millimeter