Leaf life

GUDID 06974223650011

Shenzhen Leaflife Technology Co., Ltd.

Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system Dermatological diode laser system

• Primary Device ID: 06974223650011
• NIH Device Record Key: 1d4e97e6-8bc2-4155-936a-123746b2e2ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Leaf life
• Version Model Number: LM-L808A
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn
• Phone: 9999999999
• Email: cq@leaflife.cn

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974223650011 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K202980

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2021-06-11
• Device Publish Date: 2021-06-03

On-Brand Devices [Leaf life]

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