FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOFIX

DI: 18052469476987 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ORTHOFIX
Primary DI
18052469476987
Version / Model
1
Catalog Number
700900C
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
3
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
d2f7cf0c-92e5-44ea-bd21-8ce83fcaa7d3

Device Description

FITBONE ANTEGRADE FEMUR NAIL INSTRUMENT TRAY COMPLETE

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
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 18052469476987

Customer Contacts