FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOFIX

DI: 18059015375121 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOFIX
Primary DI
18059015375121
Version / Model
1
Catalog Number
99-7245375
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-05
Public Version
4
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
e4383638-63b1-438f-a0df-2e285d5d5dd9

Device Description

REVISION LOCKING SCREW L37.5MM D4.5MM 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
No
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
HSB Rod, Fixation, Intramedullary And Accessories

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 18059015375121

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K233867 000

Device Sizes

Type Value Unit Text
Outer Diameter 4.5 Millimeter
Length 37.5 Millimeter