49199201S

GUDID H98149199201S0

1.0MM TI CABLE WITH CRIMP DOUBLE LEAD 470MM-STERILE

Synthes GmbH

Bone-screw internal spinal fixation system, sterile
Primary Device IDH98149199201S0
NIH Device Record Keydf6002f4-5f75-4130-8de4-69bfe35eb383
Commercial Distribution StatusIn Commercial Distribution
Version Model Number491.992.01S
Catalog Number49199201S
Company DUNS486711679
Company NameSynthes GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
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
GS110705034784793 [Primary]
HIBCCH98149199201S0 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDQCERCLAGE, FIXATION

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


[H98149199201S0]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-04-27
Device Publish Date2015-09-14

Devices Manufactured by Synthes GmbH

10886982348142 - NA2024-08-05 UNCANNULATED XL XL40 DRIVER
10887587078380 - NA2024-08-05 45 DEGREE TIP FLAT RIB FORCEPS, LEFT
10887587078397 - NA2024-08-05 90 DEGREE TIP FLAT RIB FORCEPS, LEFT
07612334292100 - NA2024-08-02 TRAY FOR REDUCTION AND SCREW INSERTION INSTRUMENTS
07612334292117 - NA2024-08-02 TRAY FOR LCP PLATES
07612334292124 - NA2024-08-02 SCREW CADDY
07612334292131 - NA2024-08-02 TRAY F/WIRE IMPL & INSTRUMENTS
10886982347466 - NA2024-08-02 RIGID INSERTION SLEEVE

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