FDA UDI In Commercial Distribution 🇺🇸 United States

External Fixator Sterilization box hybrid

DI: 07640136270552 · Model: 6010-1005 · GEXFIX SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
External Fixator Sterilization box hybrid
Primary DI
07640136270552
Version / Model
6010-1005
Company Name
GEXFIX SA
Labeler DUNS
482579716
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
2973ba07-6f36-4036-9425-e5a6fec5ad48

Device Description

Reusable external orthopaedic fixation system sterilization box.

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
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

GMDN Terms

Code Name
44758 General external orthopaedic fixation system implantation kit, reusable

Identifiers

Type ID
Primary 07640136270552

Premarket Submissions

Submission Number Supplement Number
K052605 000