FDA UDI In Commercial Distribution 🇺🇸 United States

FUZE

DI: 00841731120380 · Model: FTZ50-35TH · VILEX LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FUZE
Primary DI
00841731120380
Version / Model
FTZ50-35TH
Catalog Number
FTZ50-35TH
Company Name
VILEX LLC
Labeler DUNS
117502293
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-30
Public Version
4
Public Version Date
2020-05-27
Public Version Status
Update
Public Device Record Key
4afd2ee3-c35d-4ea4-ba5f-15fb8d0c682d

Device Description

Screw, FUZE 5.0x035mm_Ti Hexalobe Teal

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
HSB Rod, Fixation, Intramedullary And Accessories

GMDN Terms

Code Name
56645 Tibia nail, non-sterile

Identifiers

Type ID
Primary 00841731120380

Premarket Submissions

Submission Number Supplement Number
K102413 000