KIWI Derma

GUDID 07350120791955

KIWI Derma is blackhead suction device with microdermabrasion nozzle to remove dead skin and with T-sonic pulsation to suck out blackhead more easily.

Foreo AB

Dermabrasion brush, rotary

• Primary Device ID: 07350120791955
• NIH Device Record Key: f9d3fd48-43de-4c48-98d0-476b5212bba7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KIWI Derma
• Version Model Number: Lavender
• Company DUNS: 352394143
• Company Name: Foreo AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	07350120791955 [Primary]

FDA Product Code

• KNM: Device, Pressure Applying

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: 2024-03-19
• Device Publish Date: 2024-03-11

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