FDA UDI In Commercial Distribution 🇺🇸 United States

Galaxy Fixation System

DI: 18032937167890 · 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
18032937167890
Version / Model
1
Catalog Number
99-93040
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-06
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
7368fe4e-1e1f-48fe-a852-f2c1fe8d3f06

Device Description

LARGE DOUBLE MULTISCREW CLAMP STERILE

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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
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
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Primary 18032937167890

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113770 000