icotec Cervical Cage, Cervical Cage Anatomic, Container Lid 41-12-2

GUDID 07640164849669

icotec Cervical Cage, Cervical Cage Anatomic, Container Lid

icotec AG

Device sterilization/disinfection container, reusable

• Primary Device ID: 07640164849669
• NIH Device Record Key: 90458c3f-87f5-4bf7-b91a-be7991e31ee3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: icotec Cervical Cage, Cervical Cage Anatomic, Container Lid
• Version Model Number: 41-12-2
• Catalog Number: 41-12-2
• Company DUNS: 480789465
• Company Name: icotec AG
• 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: true
• 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: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640164849669 [Primary]

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

[07640164849669]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-10
• Device Publish Date: 2025-06-02

Devices Manufactured by icotec AG

• 07640172553848 - icotec Systems, Handle, 1/4" Coupling: 2025-08-21 icotec Systems, Handle, 1/4" Coupling
• 07640172553855 - icotec Systems, Fixation device: 2025-08-21 icotec Systems, Fixation device
• 07640172553862 - icotec Systems, Deburring tool: 2025-08-21 icotec Systems, Deburring tool
• 07640172553879 - icotec Systems, Handle for deburrer, M6: 2025-08-21 icotec Systems, Handle for deburrer, M6
• 07640172553831 - icotec Systems, Navigation Adapter: 2025-08-20 icotec Systems, Navigation Adapter
• 07640172551967 - VADER Pedicle System, Handle, 1/4" Coupling: 2025-08-07 VADER Pedicle System, Handle, 1/4" Coupling
• 07640172551981 - VADER Pedicle System, Deburring tool: 2025-08-07 VADER Pedicle System, Deburring tool
• 07640172551998 - VADER Pedicle System, Trial rod, flexible, Ø 5.5 mm; L = 300 mm: 2025-08-07 VADER Pedicle System, Trial rod, flexible, Ø 5.5 mm; L = 300 mm