NuFACE (UDI 33044)

Manufactured by Nuface

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NuFACE (Model/Catalog Number: 33044) is a medical device manufactured by Nuface. This product is indexed under FDA Product Code / Category Classification GYB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 33044
Product Code / EMDN: GYB
Device Name: Aqua Gel 1.69oz
Database Sync Date: 2026-08-09 09:37:45

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 NuFACE?

The registered manufacturer of record for NuFACE is Nuface.

What is the Primary UDI-DI identifier for NuFACE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 33044.

What classification code is assigned to this device?

This device is registered under product classification code GYB.

Similar Classification Devices (GYB)

Other Devices by Nuface

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