242107

GUDID 10886705031962

Endoscope, Mitek Lock 30 degree x 2.7 mm x 75 mm

Medos International Sàrl

Rigid arthroscope, reusable
Primary Device ID10886705031962
NIH Device Record Keyf3f56b65-3efb-4e9f-9c67-cda4f2cfd6d1
Commercial Distribution StatusIn Commercial Distribution
Version Model Number242107
Catalog Number242107
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
GS110886705031962 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EOBNasopharyngoscope (flexible or rigid)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

Moist Heat or Steam Sterilization


[10886705031962]

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

Devices Manufactured by Medos International Sàrl

10705034595542 - TRIALTIS2024-08-26 TRIALTIS Spine System Set Screw 4 Pack T27 5.5 and 6.0
10705034595887 - TRIALTIS2024-08-26 TRIALTIS Spine System Set Screw 8 Pack T27 5.5 and 6.0
10705034596891 - TRIALTIS2024-08-26 TRIALTIS Spine System Set Screw 2 Pack T27 5.5 and 6.0
10705034596907 - TRIALTIS2024-08-26 TRIALTIS Spine System Set Screw 6 Pack T27 5.5 and 6.0
10705034199504 - VIPER2024-08-20 VIPER SYSTEM CANNULA PLUNGER
10705034062358 - MONARCH2024-07-29 MONARCH SPINE SYSTEM S/C WITH WASHER, STRAIGHT 5.5mm
10705034062365 - MONARCH2024-07-29 MONARCH SPINE SYSTEM S/C WITH WASHER, EXT 5.5mm
10705034062372 - MONARCH2024-07-29 MONARCH SPINE SYSTEM SLOTTED CONNECTOR WITH WASHER, OFFSET, RIGHT 5.5mm

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.