163005540

GUDID 10705034507385

CONCORDE Clear MIS DISCECTOMY DEVICE 5MM, 40 DEGREES

Medos International Sàrl

Surgical/emergency suction cannula, non-illuminating, single-use

• Primary Device ID: 10705034507385
• NIH Device Record Key: 3e61f2a5-d7c9-4089-922c-4e9e4efbd831
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 163005540
• Catalog Number: 163005540
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034507385 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122861

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-10-12
• Device Publish Date: 2016-10-13

Devices Manufactured by Medos International Sàrl

• 10705034604527 - TELIGEN: 2024-12-17 TELIGEN ACCESS PROBE
• 10705034604558 - TELIGEN: 2024-12-17 TELIGEN ACCESS PROBE WITH STIMULATION WIRE
• 10705034595542 - TRIALTIS: 2024-08-26 TRIALTIS Spine System Set Screw 4 Pack T27 5.5 and 6.0
• 10705034595887 - TRIALTIS: 2024-08-26 TRIALTIS Spine System Set Screw 8 Pack T27 5.5 and 6.0
• 10705034596891 - TRIALTIS: 2024-08-26 TRIALTIS Spine System Set Screw 2 Pack T27 5.5 and 6.0
• 10705034596907 - TRIALTIS: 2024-08-26 TRIALTIS Spine System Set Screw 6 Pack T27 5.5 and 6.0
• 10705034199504 - VIPER: 2024-08-20 VIPER SYSTEM CANNULA PLUNGER
• 10705034062358 - MONARCH: 2024-07-29 MONARCH SPINE SYSTEM S/C WITH WASHER, STRAIGHT 5.5mm