FDA UDI In Commercial Distribution 🇺🇸 United States

SOLE MEDIAL COLUMN FUSION PLATE

DI: 18052469470800 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SOLE MEDIAL COLUMN FUSION PLATE
Primary DI
18052469470800
Version / Model
1
Catalog Number
99-M314M
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-03
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
6375c72a-e946-4df7-9054-123881017657

Device Description

SELF DRILLING CORTICAL SCREW L70/20MM D3.0-2.5MM PACK OF 2 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
Yes
PM Exempt
Yes
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
HTO Reamer

GMDN Terms

Code Name
32854 Orthopaedic bone pin, non-bioabsorbable

Identifiers

Type ID
Primary 18052469470800

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 3 Millimeter
Length 70 Millimeter