VADER Pedicle System VADER Pedicle System 1/2 Container Inlay 42-851-3

GUDID 07640172552155

VADER Pedicle System VADER Pedicle System 1/2 Container Inlay

icotec AG

Device sterilization/disinfection container, reusable

• Primary Device ID: 07640172552155
• NIH Device Record Key: f16f9a82-4e44-4509-a07f-ef7e0c7e638e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VADER Pedicle System VADER Pedicle System 1/2 Container Inlay
• Version Model Number: 42-851-3
• Catalog Number: 42-851-3
• 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	07640172552155 [Primary]

FDA Product Code

• NKB: Thoracolumbosacral Pedicle Screw System

Sterilization

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

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

Moist Heat or Steam Sterilization

[07640172552155]

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

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• 07640172552551 - CMORE® System, Pedicle Probe, Straight: 2025-12-02 CMORE® System, Pedicle Probe, Straight
• 07640172552568 - CMORE® System, Drill Guide Sleeve: 2025-12-02 CMORE® System, Drill Guide Sleeve
• 07640172552575 - CMORE® System, Drill Guide Stop: 2025-12-02 CMORE® System, Drill Guide Stop
• 07640172552582 - CMORE® System, Drill Bit, Ø 2.3 mm: 2025-12-02 CMORE® System, Drill Bit, Ø 2.3 mm
• 07640172552599 - CMORE® System, Feeler: 2025-12-02 CMORE® System, Feeler
• 07640172552605 - CMORE® System, In-line Handle, AO Coupling: 2025-12-02 CMORE® System, In-line Handle, AO Coupling