FDA UDI Not in Commercial Distribution 🇺🇸 United States

TECHFIT

DI: 00860012759446 · Model: 0 · Techfit Digital Surgery, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TECHFIT
Primary DI
00860012759446
Version / Model
0
Catalog Number
GCPTI
Company Name
Techfit Digital Surgery, Inc.
Labeler DUNS
117050279
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-17
Public Version
2
Public Version Date
2026-04-03
Public Version Status
Update
Public Device Record Key
8c470085-5975-4d7f-ae28-cad93579b30d
Distribution End Date
2026-04-02

Device Description

Fibula cutting guide Ti

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
Yes
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
DZJ Driver, Wire, And Bone Drill, Manual
LLZ System, Image Processing, Radiological

GMDN Terms

Code Name
60826 Custom-made orthopaedic/craniofacial surgical guide

Identifiers

Type ID
Primary 00860012759446