FDA UDI In Commercial Distribution 🇺🇸 United States

TOMOFIX

DI: 10886982188069 · Model: 312.930 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
TOMOFIX
Primary DI
10886982188069
Version / Model
312.930
Catalog Number
312930
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
4
Public Version Date
2023-09-01
Public Version Status
Update
Public Device Record Key
202c3012-3107-428e-9539-7125dee43eef

Device Description

TOMOFIX(TM) GUIDING BLOCK FOR LATERAL HIGH TIBIA-RIGHT

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
No
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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
61929 Orthopaedic implant aiming/guiding block attachment tool

Identifiers

Type ID
Direct Marking 07611819256125
Secondary H6793129300
Primary 10886982188069

Customer Contacts