Leaf life

GUDID 06974223650028

Shenzhen Leaflife Technology Co., Ltd.

Intense pulsed light skin surface treatment system

• Primary Device ID: 06974223650028
• NIH Device Record Key: 9749f3e1-6bbe-490a-9da9-781c17cc93d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Leaf life
• Version Model Number: LH-LIPLB
• Company DUNS: 419291256
• Company Name: Shenzhen Leaflife 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: false
• 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	06974223650028 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212697

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: 2022-11-11
• Device Publish Date: 2022-11-03

On-Brand Devices [Leaf life]

• 06974223650011: LM-L808A
• 06974223650028: LH-LIPLB
• 06974223650004: LM-LNIRA