VELOFIX™ PEEK LUMBAR CAGE

GUDID 08800308485750

CG MedTech Co.,Ltd.

Instrument tray, reusable

• Primary Device ID: 08800308485750
• NIH Device Record Key: b044fb66-39bb-4186-847a-8efbf61cccbe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VELOFIX™ PEEK LUMBAR CAGE
• Version Model Number: PL0910
• Company DUNS: 688811082
• Company Name: CG MedTech Co.,Ltd.
• 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: 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	08800308485750 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

[08800308485750]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-01-06
• Device Publish Date: 2025-12-29

On-Brand Devices [VELOFIX™ PEEK LUMBAR CAGE]

• 08800308485767: PL0914
• 08800308485750: PL0910