VitaPeel 33-0016

GUDID 00686209330164

microdermabrasion skin care device

Dectro International

Multi-modality skin surface treatment system

• Primary Device ID: 00686209330164
• NIH Device Record Key: 743f1aec-943f-4e98-bd6c-1a13e9709eee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VitaPeel
• Version Model Number: Safina Pro
• Catalog Number: 33-0016
• 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	00686209330164 [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: 2024-05-31
• Device Publish Date: 2024-05-23

On-Brand Devices [VitaPeel]

• 00686209330164: microdermabrasion skin care device
• 00686209330140: microdermabrasion skin care device