Aymo

GUDID 16973504240009

IPL HAIR REMOVAL DEVICE

Medical Device Branch of Zhangzhou Easepal Industrial Corporation

Multi-modality skin surface treatment system

• Primary Device ID: 16973504240009
• NIH Device Record Key: 112afe00-346c-49fb-8101-c1f5396fbd90
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aymo
• Version Model Number: Aymo Beauty D50 148Q-BD50XX-USWH0A
• Company DUNS: 554415413
• Company Name: Medical Device Branch of Zhangzhou Easepal Industrial Corporation
• Device Count: 1
• DM Exempt: true
• 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: true
• Serial Number: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973504240002 [Primary]
GS1	16973504240009 [Package]; Contains: 06973504240002; Package: [10 Units]; In Commercial Distribution

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: 2021-05-28
• Device Publish Date: 2021-05-20

On-Brand Devices [Aymo]

• 16973504240016: IPL HAIR REMOVAL DEVICE
• 16973504240009: IPL HAIR REMOVAL DEVICE