TOMOFIX 312924

GUDID 07611819941885

TOMOFIX GUIDING BLOCK F/MEDIAL HIGH TIBIA PLATE-SMALL

Synthes GmbH

Orthopaedic implant aiming/guiding block, reusable
Primary Device ID07611819941885
NIH Device Record Keyea7944fc-65c7-40ab-ae62-db83928f4907
Commercial Distribution StatusIn Commercial Distribution
Brand NameTOMOFIX
Version Model Number312.924
Catalog Number312924
Company DUNS486711679
Company NameSynthes GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
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Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS107611819941885 [Direct Marking]
GS110886982188045 [Primary]
HIBCCH6793129240 [Secondary]

FDA Product Code

FZXGuide, surgical, instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


[07611819941885]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-04-29
Device Publish Date2016-12-31

On-Brand Devices [TOMOFIX]

H679031200690TOMOFIX GUIDING BLOCK FOR MEDIAL DISTAL FEMUR PLATE-LT
H679031200680TOMOFIX GUIDING BLOCK FOR MEDIAL DISTAL FEMUR PLATE-RT
07611819256156TOMOFIX(TM) GUIDING BLOCK FOR LATERAL DISTAL FEMUR-LEFT
07611819256149TOMOFIX(TM) GUIDING BLOCK FOR LATERAL DISTAL FEMUR-RIGHT
07611819256132TOMOFIX(TM) GUIDING BLOCK FOR LATERAL HIGH TIBIA-LEFT
07611819256125TOMOFIX(TM) GUIDING BLOCK FOR LATERAL HIGH TIBIA-RIGHT
07611819256118TOMOFIX(TM) GUIDING BLOCK FOR MEDIAL HIGH TIBIA
07611819941885TOMOFIX GUIDING BLOCK F/MEDIAL HIGH TIBIA PLATE-SMALL
H67904120551S0TI TOMOFIX MEDIAL DISTAL FEMUR PL/4 HOLES/LEFT-STERILE
H679041205510TI TOMOFIX MEDIAL DISTAL FEMUR PLATE - 4 HOLES/LEFT
H67904120550S0TI TOMOFIX MEDIAL DISTAL FEMUR PL/4 HOLES/RIGHT-STERILE
H679041205500TI TOMOFIX MEDIAL DISTAL FEMUR PLATE - 4 HOLES/RIGHT
H6796712980SYNCASE FOR TOMOFIX(TM) SCREW SET
H6796712940SYNCASE FOR TOMOFIX(TM) INSTRUMENT SET
H679601200500TOMOFIX INSTRUMENT AND TI IMPLANT SET GRAPHIC CASE
H6794408740TI TOMOFIX(TM) LATERAL DISTAL FEMUR PLATE-4 HOLES/LEFT
H6794408640TI TOMOFIX(TM) LATERAL DISTAL FEMUR PLATE-4 HOLES/RIGHT
H6794408530TI TOMOFIX(TM) LATERAL HIGH TIBIA PLATE-3 HOLES/LEFT
H6794408430TI TOMOFIX(TM) LATERAL HIGH TIBIA PLATE-3 HOLES/RIGHT
H6794408340TI TOMOFIX(TM) MEDIAL HIGH TIBIA PLATE-4 HOLES
H6794408310TI TOMOFIX MEDIAL HIGH TIBIA PLATE-4 HOLES/SMALL
07611819275737TOMOFIX OSTEOTOMY CHISEL 25MM WIDTH
07611819275720TOMOFIX OSTEOTOMY CHISEL 20MM WIDTH
07611819275713TOMOFIX OSTEOTOMY CHISEL 15MM WIDTH
07611819275706TOMOFIX OSTEOTOMY CHISEL 10MM WIDTH
07611819284951TOMOFIX(TM) OSTEOTOMY GAP MEASURING DEVICE
07611819278721TOMOFIX(TM) BONE SPREADER

Trademark Results [TOMOFIX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TOMOFIX
TOMOFIX
76467177 2981413 Live/Registered
DEPUY SYNTHES, INC.
2002-11-05

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