Medi Lift

GUDID 10850021950023

This device is a wearable facial stimulation device for over-the-counter cosmetic use.

YA-MAN LTD.

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 10850021950023
• NIH Device Record Key: e5ab406e-2346-4693-9954-9f6c0e027282
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medi Lift
• Version Model Number: EPM-18-GC
• Company DUNS: 690652508
• Company Name: YA-MAN 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: false
• 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	00850021950026 [Primary]
GS1	10850021950023 [Package]; Contains: 00850021950026; Package: [24 Units]; In Commercial Distribution

FDA Product Code

• NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes

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: 2023-08-07
• Device Publish Date: 2023-07-28

On-Brand Devices [Medi Lift]

• 10850021950023: This device is a wearable facial stimulation device for over-the-counter cosmetic use.
• 10850021950016: This device is a wearable facial stimulation device for over-the-counter cosmetic use.
• 10850021950009: This device is a wearable facial stimulation device for cosmetic use.