242094

GUDID 10886705031900

Endoscope, Mitek Lock 0 degree x 1.9 mm x 60 mm

Medos International Sàrl

Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid 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 Rigid optical arthroscope, reusable
Primary Device ID10886705031900
NIH Device Record Key7bc3cbd2-270b-4c0f-bff6-a3d0a75fb8ed
Commercial Distribution StatusIn Commercial Distribution
Version Model Number242094
Catalog Number242094
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
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
GS110886705031900 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


[10886705031900]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-28
Device Publish Date2021-05-20

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10705034507828 - VIPER PRIME2024-04-11 VIPER PRIME NAVIGATION STYLET
10886705012367 - COR2024-03-27 COR Disposable Kit, 6mm
10886705012374 - COR2024-03-27 COR Disposable Kit, 8mm
10886705012381 - COR2024-03-27 COR Disposable Kit, 10mm
10886705012404 - COR2024-03-27 COR Disposable Kit, 8mm w/Perpendicularity
10886705012398 - COR2024-03-18 COR Disposable Kit, 6mm w/Perpendicularity
10886705012411 - COR2024-03-18 COR Disposable Kit, 10mm w/Perpendicularity

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