289215111

GUDID 10705034548241

ATP/Lateral Discectomy Instruments Lateral Angled Cobb Elevator Right, Navigable Angled 20mm

Medos International Sàrl

Bone lever/elevator, reusable

• Primary Device ID: 10705034548241
• NIH Device Record Key: 64efdd9c-3627-4ebe-a8d0-e0d2b1064b38
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 289215111
• Catalog Number: 289215111
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034548241 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212756

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

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

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

[10705034548241]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-17
• Device Publish Date: 2022-08-09

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• 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