163005630

GUDID 10705034507408

CONCORDE Clear MIS DISCECTOMY DEVICE 6MM, 30 DEGREES

Medos International Sàrl

Surgical/emergency suction cannula, non-illuminating, single-use
Primary Device ID10705034507408
NIH Device Record Key36cabed7-8ddd-4f07-a6f9-64897e657c39
Commercial Distribution StatusIn Commercial Distribution
Version Model Number163005630
Catalog Number163005630
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
GS110705034507408 [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

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
10705034062396 - MONARCH2024-07-29 MONARCH SPINE SYSTEM SLOTTED CONNECTOR WITH WASHER, OFFSET, LEFT 5.5mm
10705034584881 - TRIALTIS2024-07-26 TRIALTIS Spine System Polyaxial Favored Angle Screw Fenestrated ø10mm x 60mm 5.5 and 6.0
10705034032108 - EXPEDIUM2024-07-24 EXPEDIUM SPINE SYSTEM SPINAL WIRE WITH BUTTON Diameter 1.0mm
10705034032115 - EXPEDIUM2024-07-24 EXPEDIUM SPINE SYSTEM SPINAL WIRE, DOUBLE Diameter 1.0mm
10705034032122 - EXPEDIUM2024-07-24 EXPEDIUM SPINE SYSTEM SPINAL WIRE, SINGLE Diameter 1.0mm

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