FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOFIX

DI: 18052469476499 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOFIX
Primary DI
18052469476499
Version / Model
1
Catalog Number
700270
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
90a2806e-433d-47aa-a100-846c0da4f83b

Device Description

ENTRY REAMER D12MM

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
HTO Reamer

GMDN Terms

Code Name
45115 Medullary canal orthopaedic reamer, rigid

Identifiers

Type ID
Primary 18052469476499

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 14 Millimeter
Outer Diameter 12 Millimeter
Lumen/Inner Diameter 3.5 Millimeter