163005540

GUDID 10705034507385

CONCORDE Clear MIS DISCECTOMY DEVICE 5MM, 40 DEGREES

Medos International Sàrl

Surgical/emergency suction cannula, non-illuminating, single-use
Primary Device ID10705034507385
NIH Device Record Key3e61f2a5-d7c9-4089-922c-4e9e4efbd831
Commercial Distribution StatusIn Commercial Distribution
Version Model Number163005540
Catalog Number163005540
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110705034507385 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXARTHROSCOPE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-10-12
Device Publish Date2016-10-13

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

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