FDA UDI In Commercial Distribution 🇺🇸 United States

PRO-TOE

DI: 00840420123022 · Model: 45712000 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PRO-TOE
Primary DI
00840420123022
Version / Model
45712000
Catalog Number
45712000
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-01
Public Version
8
Public Version Date
2025-02-06
Public Version Status
Update
Public Device Record Key
2364d5ae-f8a1-47da-89b8-af47de7d177a

Device Description

VO Blade

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
HWC Screw, fixation, bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 00840420123022

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 2 Millimeter
Length 13 Millimeter
Angle 0 degree