EVE Ace of Face

GUDID 08809851470060

WEERO Co., Ltd.

Multi-modality skin surface treatment system

• Primary Device ID: 08809851470060
• NIH Device Record Key: dbcd9a43-77e8-422b-b9de-bbb59022273d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EVE Ace of Face
• Version Model Number: EVE-1000
• Company DUNS: 963224510
• Company Name: WEERO Co., Ltd.
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809851470060 [Primary]

FDA Product Code

• GFE: Brush, Dermabrasion, Powered

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: 2024-07-22
• Device Publish Date: 2024-07-12

Devices Manufactured by WEERO Co., Ltd.

• 08809851470053 - eMVFit: 2024-10-30 Pain management device with RF, Vacuum and EMS
• 08809851470060 - EVE Ace of Face: 2024-07-22
• 08809851470060 - EVE Ace of Face: 2024-07-22