301019014

GUDID 10705034561325

NAVIGATION ENABLED INSTRUMENTS DUAL LEAD CANNULATED TAP 4.35MM

Medos International Sàrl

Bone tap, reusable
Primary Device ID10705034561325
NIH Device Record Keyf247506e-df4d-4180-9ad0-ed18e690acca
Commercial Distribution StatusIn Commercial Distribution
Version Model Number3010-19-014
Catalog Number301019014
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
GS110705034561325 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OLOOrthopedic stereotaxic instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

Moist Heat or Steam Sterilization


[10705034561325]

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

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10705034643267 - VELYS2025-04-07 VELYS™ SCREWDRIVER T20
10705034643274 - VELYS2025-04-07 VELYS SPINE ARRAY BASE SET
10705034643281 - VELYS2025-04-07 VELYS BURR ADAPTOR
10705034643298 - VELYS2025-04-07 VELYS SPINE CERVICAL CLAMP L
10705034643304 - VELYS2025-04-07 VELYS SPINE CERVICAL CLAMP S
10705034643311 - VELYS2025-04-07 VELYS SPINE INSTRUMENT TRAY 1

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