242009

GUDID 10886705028788

HD EP Arthroscope/Sinuscope compatible with Storz style 4.0mm x 70 deg x 175mm

Medos International Sàrl

Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable
Primary Device ID10886705028788
NIH Device Record Key9dc52c08-6404-40be-b5ba-3e483f256b6c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number242009
Catalog Number242009
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 Batchfalse
Serial Numbertrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110886705028788 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EOBNASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


[10886705028788]

Moist Heat or Steam Sterilization;Hydrogen Peroxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-11-17
Device Publish Date2017-07-21

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