242364

GUDID 10886705029259

ADAPTOR ACMI INSTRUMENT UNIVERSAL TIP

Medos International Sàrl

Light source adaptor
Primary Device ID10886705029259
NIH Device Record Key7fafed6a-0d69-41ed-b004-d77d4e0fd528
Commercial Distribution StatusIn Commercial Distribution
Version Model Number242364
Catalog Number242364
Company DUNS482661753
Company NameMedos International Sàrl
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
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
GS110886705029259 [Primary]

FDA Product Code

FSTLIGHT, SURGICAL, FIBEROPTIC
FSXLight, surgical, connector

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-02-17
Device Publish Date2022-02-09

Devices Manufactured by Medos International Sàrl

10705034587486 - TRIALTIS2025-08-06 TRIALTIS Spine System Closed Lateral Connector Adjustable ø5.5-6.35mm to 5.5mm x 20mm
10705034587509 - TRIALTIS2025-08-06 TRIALTIS Spine System Closed Lateral Connector Adjustable ø5.5-6.35mm to 5.5mm x 40mm
10705034587516 - TRIALTIS2025-08-06 TRIALTIS Spine System Closed Lateral Connector Adjustable ø5.5-6.35mm to 5.5mm x 60mm
10705034587547 - TRIALTIS2025-08-06 TRIALTIS Spine System Closed Lateral Connector Fixed ø5.5-6.35mm to 5.5mm x 20mm
10705034584188 - TRIALTIS2025-07-25 TRIALTIS Spine System Side by Side Connector,Short Side Loading / Side Loading ø5.5-6.35mm to 5.5-6.35mm
10705034584195 - TRIALTIS2025-07-25 TRIALTIS Spine System Side by Side Connector,Standard Side Loading / Side Loading ø5.5-6.35mm to 5.5-6.35mm
10705034584201 - TRIALTIS2025-07-25 TRIALTIS Spine System Side by Side Connector,Long Side Loading / Side Loading ø5.5-6.35mm to 5.5-6.35mm
10705034584218 - TRIALTIS2025-07-25 TRIALTIS Spine System Double Side by Side Connector,Short Side Loading / Side Loading ø5.5-6.35mm to 5.5-6.35mm

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.