gudid Primary ID: 120V, Black

Hydrafacial Syndeo (UDI 120V, Black)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Hydrafacial Syndeo (Model/Catalog Number: 120V, Black) is a medical device manufactured by Hydrafacial LLC. This product is indexed under FDA Product Code / Category Classification GFE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 120V, Black
Product Code / EMDN: GFE
Device Name: 100-120VAC, 50/60Hz, 2A
Database Sync Date: 2026-08-09 09:17:12

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 Hydrafacial Syndeo?

The registered manufacturer of record for Hydrafacial Syndeo is Hydrafacial LLC.

What is the Primary UDI-DI identifier for Hydrafacial Syndeo?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 120V, Black.

What classification code is assigned to this device?

This device is registered under product classification code GFE.

Similar Classification Devices (GFE)

Other Devices by Hydrafacial LLC

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