IPL Hair Removal Device

GUDID 06976901787835

Dongguan Lide Elentric Appliance Co., Ltd

Home-use intense pulsed light hair removal unit

• Primary Device ID: 06976901787835
• NIH Device Record Key: ba3fc965-967a-4f82-96bf-f1bab951a272
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IPL Hair Removal Device
• Version Model Number: PB3
• Company DUNS: 844962327
• Company Name: Dongguan Lide Elentric Appliance 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06976901787835 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232056

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: 2024-05-14
• Device Publish Date: 2024-05-06

On-Brand Devices [IPL Hair Removal Device]

• 06976901787859: TM002
• 06976901787842: PB4
• 06976901787835: PB3
• 06976901787828: PB2
• 06976901787811: PB1