Idys™- ALIF 24704000

GUDID 03700780638734

RASP

CLARIANCE

Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 03700780638734
• NIH Device Record Key: 88765df3-9337-4d5e-8bca-c50a3e60c6f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Idys™- ALIF
• Version Model Number: 24704000
• Catalog Number: 24704000
• Company DUNS: 296568400
• Company Name: CLARIANCE
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us
• Phone: +1 773 868 7041
• Email: s.chambat@clariance-spine.us

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700780638734 [Primary]

FDA Product Code

• HTR: Rasp

Sterilization

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

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

[03700780638734]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-23
• Device Publish Date: 2023-03-15

Devices Manufactured by CLARIANCE

• 03700780644018 - Idys®- C ZP 3DTi: 2024-04-04 SCREW
• 03700780644025 - Idys®- C ZP 3DTi: 2024-04-04 SCREW
• 03700780644032 - Idys®- C ZP 3DTi: 2024-04-04 SCREW
• 03700780644049 - Idys®- C ZP 3DTi: 2024-04-04 SCREW
• 03700780644186 - Idys®- C ZP 3DTi: 2024-04-04 SCREW
• 03700780644193 - Idys®- C ZP 3DTi: 2024-04-04 SCREW
• 03700780644209 - Idys®- C ZP 3DTi: 2024-04-04 SCREW
• 03700780644216 - Idys®- C ZP 3DTi: 2024-04-04 SCREW