Nood

GUDID 06975587680003

Hunan Guangye Biotechnology Co., Ltd.

Home-use intense pulsed light hair removal unit

• Primary Device ID: 06975587680003
• NIH Device Record Key: d31d2823-caaa-49e3-8eb3-fd371a4d3e50
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nood
• Version Model Number: KCA423
• Company DUNS: 404145347
• Company Name: Hunan Guangye 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975587680003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K210119

FDA Product Code

• ONF: Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

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: 2022-07-26
• Device Publish Date: 2022-07-18

On-Brand Devices [Nood]

• 06975587680003: KCA423
• 06975587680034: KCA423