03311047

GUDID H679033110470

REDUCTION WIRE 1.8MM DIA HALF POINT TIP

Synthes GmbH

Orthopaedic bone wire
Primary Device IDH679033110470
NIH Device Record Key31cceb08-3cf0-49c3-8144-8ee34bde5e15
Commercial Distribution StatusIn Commercial Distribution
Version Model Number03.311.047
Catalog Number03311047
Company DUNS486711679
Company NameSynthes GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
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
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
GS110886982078063 [Primary]
HIBCCH679033110470 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


[H679033110470]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-05-27
Device Publish Date2015-09-14

Devices Manufactured by Synthes GmbH

10886982348982 - NA2025-07-24 Ø12.8MM HOLLOW REAMER
10886982349835 - NA2025-07-24 WRENCH / 11MM SLOTTED SOCKET
10886982350121 - NA2025-07-24 FEMORAL GONIOMETER
10886982350152 - NA2025-07-24 5TH MET WIRE GUIDE
10886982350428 - NA2025-07-24 TENS BENDING EXTRACTOR
10886982348326 - NA2025-07-08 SCREW RACK 3.0 & 4.0
10887587078434 - NA2025-07-03 REDUCTION FORCEPS W/ POINTS
10886982343994 - NA2025-07-01 Ø14MM HOLLOW REAMER - FRN

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.