Curaway

GUDID 06936666590651

Radiofrequency Generator System

Zhejiang CuraWay Medical Technology Co., Ltd.

Percutaneous radio-frequency ablation system generator

• Primary Device ID: 06936666590651
• NIH Device Record Key: b9a7a203-c011-4c79-a373-bbbefa12a56e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curaway
• Version Model Number: CR-S2000
• Company DUNS: 412923111
• Company Name: Zhejiang CuraWay Medical Technology 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	06936666590651 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240758

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2025-08-19
• Device Publish Date: 2025-08-11

On-Brand Devices [Curaway]

• 06936666590651: Radiofrequency Generator System
• 06936666559269: Endovenous Radiofrequency Generator
• 06936666557944: Irreversible Electroporation Ablation Generator