163005615

GUDID 10705034507392

CONCORDE Clear MIS DISCECTOMY DEVICE 6MM, 15 DEGREES

Medos International Sàrl

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

• Primary Device ID: 10705034507392
• NIH Device Record Key: d8a745c9-682c-4fec-af3a-5d1a95ae6cec
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 163005615
• Catalog Number: 163005615
• 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	10705034507392 [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

• 10705034643243 - VELYS: 2025-04-07 VELYS™ PATIENT ARRAY CONNECTOR
• 10705034643250 - VELYS: 2025-04-07 VELYS™ POINTER
• 10705034643267 - VELYS: 2025-04-07 VELYS™ SCREWDRIVER T20
• 10705034643274 - VELYS: 2025-04-07 VELYS SPINE ARRAY BASE SET
• 10705034643281 - VELYS: 2025-04-07 VELYS BURR ADAPTOR
• 10705034643298 - VELYS: 2025-04-07 VELYS SPINE CERVICAL CLAMP L
• 10705034643304 - VELYS: 2025-04-07 VELYS SPINE CERVICAL CLAMP S
• 10705034643311 - VELYS: 2025-04-07 VELYS SPINE INSTRUMENT TRAY 1