IPL Hair Removal Device

GUDID 06977322930008

Shenzhen Yuwei Electronic Technology Co., Ltd.

Home-use intense pulsed light hair removal unit

• Primary Device ID: 06977322930008
• NIH Device Record Key: b64bb307-1b29-49c0-8b98-b5464842f394
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IPL Hair Removal Device
• Version Model Number: S1
• Company DUNS: 709757825
• Company Name: Shenzhen Yuwei Electronic 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: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06977322930008 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220222

FDA Product Code

• OHT: Light Based Over-The-Counter Hair Removal

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: 2024-05-31
• Device Publish Date: 2024-05-23

On-Brand Devices [IPL Hair Removal Device]

• 06977322930039: S4
• 06977322930022: S3
• 06977322930015: S2
• 06977322930008: S1