Caduceus S

GUDID 24719878713058

Taiwan Main Orthopaedic Biotechnology Co., Ltd.

Surgical planning/navigation-enhancement system

• Primary Device ID: 24719878713058
• NIH Device Record Key: 75e4ee52-5384-4c9c-8a6e-be79fdfc9972
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Caduceus S
• Version Model Number: CDS-02
• Company DUNS: 658875222
• Company Name: Taiwan Main Orthopaedic Biotechnology Co., Ltd.
• 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: false
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	24719878713058 [Primary]

FDA Product Code

• SBF: Orthopedic Augmented Reality

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-21
• Device Publish Date: 2025-01-13

On-Brand Devices [Caduceus S]

• 24719878713041: CDS-02
• 24719878713065: CDS-02
• 24719878713058: CDS-02