FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOFIX

DI: 18059015372908 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOFIX
Primary DI
18059015372908
Version / Model
1
Catalog Number
60003517
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-30
Public Version
4
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
408210cf-422d-46b4-b179-662d3077e39b

Device Description

FITBONE TLN SCREW OVERLAY

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 Unsafe
Direct Marking Exempt
No
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
FTY Tape, Measuring, Rulers And Calipers

GMDN Terms

Code Name
44796 Medical ruler, reusable

Identifiers

Type ID
Primary 18059015372908

Customer Contacts