301019020

GUDID 10705034561226

NAVIGATION ENABLED INSTRUMENTS DUAL LEAD CANNULATED TAP 10MM

Medos International Sàrl

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Primary Device ID10705034561226
NIH Device Record Key15438853-8c38-449c-8e6f-84b2ec047894
Commercial Distribution StatusIn Commercial Distribution
Version Model Number3010-19-020
Catalog Number301019020
Company DUNS482661753
Company NameMedos International Sàrl
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 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
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
GS110705034561226 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OLOOrthopedic stereotaxic instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


[10705034561226]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-29
Device Publish Date2020-10-21

Devices Manufactured by Medos International Sàrl

10705034031767 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM BAND CLAMP WITH WASHER 6.35mm
10705034031781 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM SLOTTED CONNECTOR WITH WASHERS, STRAIGHT 5.5/6.35mm
10705034031798 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM SLOTTED CONNECTOR WITH WASHERS, EXTENDED 5.5/6.35mm
10705034031811 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM SLOTTED CONNECTOR WITH WASHER, MINI-OFFSET, RIGHT 5.5/6.35mm
10705034031835 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM SLOTTED CONNECTOR WITH WASHER, MINI-OFFSET, LEFT 5.5/6.35mm
10705034032429 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM POLYAXIAL WASHER
10705034032436 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM WASHER, SPACER 2mm
10705034070094 - EXPEDIUM2024-07-17 EXPEDIUM SPINE SYSTEM DI WASHER 5.5

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