gudid Primary ID: Pro Max System 110V black

PRO MAX, System, 110V (UDI Pro Max System 110V black)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The PRO MAX, System, 110V (Model/Catalog Number: Pro Max System 110V black) is a medical device manufactured by ENDYMED MEDICAL LTD. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Pro Max System 110V black
Product Code / EMDN: GEI
Device Name: ENDYMED PRO MAX is a computerized system that generates pulses of radio frequency (RF) energythat are emitted onto patient skin. The device consists of a console and seven handpieces that emiteither ablative or non-ablative radiofrequency.The PRO MAX system is a RF device intended for use in dermatologic procedures with separate indications for each handpiece
Database Sync Date: 2026-08-09 09:18:18

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of PRO MAX, System, 110V?

The registered manufacturer of record for PRO MAX, System, 110V is ENDYMED MEDICAL LTD.

What is the Primary UDI-DI identifier for PRO MAX, System, 110V?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Pro Max System 110V black.

What classification code is assigned to this device?

This device is registered under product classification code GEI.

Similar Classification Devices (GEI)

Other Devices by ENDYMED MEDICAL LTD

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