Apilus 01-0123US

GUDID 00686209101238

needle-type epilator

Dectro International

Professional hair-removal electrolysis system

• Primary Device ID: 00686209101238
• NIH Device Record Key: 6ebe8ed3-b88a-461e-b777-9257d3679dfb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Apilus
• Version Model Number: Senior 3G
• Catalog Number: 01-0123US
• Company DUNS: 246237945
• Company Name: Dectro International
• 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: 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	00686209101238 [Primary]

FDA Product Code

• KCW: Epilator, High Frequency, Needle-Type

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: 2024-05-30
• Device Publish Date: 2024-05-22

On-Brand Devices [Apilus]

• 00686209101238: needle-type epilator
• 00686209106059: needle-type epilator
• 00686209106004: needle-type epilator
• 00686209101115: needle-type epilator
• 00686209100910: needle-type epilator
• 00686209100903: needle-type epilator