ANAX™ OCT SPINAL SYSTEM

GUDID 08800037598165

CG MedTech Co.,Ltd.

Orthopaedic implant driver

• Primary Device ID: 08800037598165
• NIH Device Record Key: 4ca3e7e9-d8d5-47a6-8af4-e93b964b4b2f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ANAX™ OCT SPINAL SYSTEM
• Version Model Number: OSS0680
• 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	08800037598165 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

[08800037598165]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-02-27
• Device Publish Date: 2025-02-19

On-Brand Devices [ANAX™ OCT SPINAL SYSTEM]

• 08800247357194: OS0420
• 08800247357187: OS0410
• 08800037598165: OSS0680
• 08800308480069: OS0240