Zemits Verstand HD

GUDID 00860010841136

Advance-Esthetic LLC

Multi-modality skin surface treatment system

• Primary Device ID: 00860010841136
• NIH Device Record Key: 1e3bd81b-e9ab-434a-a3de-7ab7ab7ff4e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zemits Verstand HD
• Version Model Number: 1
• Company DUNS: 043911204
• Company Name: Advance-Esthetic LLC
• 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: true
• 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

Customer Support Contacts

• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us
• Phone: 8889993996
• Email: customer-support@advance-esthetic.us

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860010841136 [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: 2024-02-05
• Device Publish Date: 2024-01-27

Devices Manufactured by Advance-Esthetic LLC

• 00860010841174 - Zemits DuoCratus: 2024-02-14
• 00860010841112 - Zemits Klein EL: 2024-02-05
• 00860010841129 - Zemits Klein RF: 2024-02-05
• 00860010841136 - Zemits Verstand HD: 2024-02-05
• 00860010841136 - Zemits Verstand HD: 2024-02-05
• 00860010841143 - Zemits JoliPeel: 2024-02-05
• 00860010841150 - Zemits CelluSpice Pro: 2024-02-05
• 00860010841167 - Zemits OxiVelour: 2024-02-05
• 00860009982413 - Zemits CrystalFrax: 2023-09-25