FDA UDI Not in Commercial Distribution 🇺🇸 United States

ORTHOFIX

DI: 18059015373660 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOFIX
Primary DI
18059015373660
Version / Model
1
Catalog Number
99-709265
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-05
Public Version
5
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
0a61e95b-e13f-44d1-a5b4-ad6968c8da17
Distribution End Date
2024-10-04

Device Description

FITBONE TROCHANTERIC NAIL L265MM D9MM 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
MR Unsafe
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
63191 Long bone distraction intramedullary nail, motorized

Identifiers

Type ID
Primary 18059015373660

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K233867 000

Device Sizes

Type Value Unit Text
Outer Diameter 9 Millimeter
Outer Diameter 10 Millimeter
Length 265 Millimeter