gudid Primary ID: TheraFace Hot & Cold Rings Black

TheraFace (UDI TheraFace Hot & Cold Rings Black)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The TheraFace (Model/Catalog Number: TheraFace Hot & Cold Rings Black) is a medical device manufactured by Therabody, Inc.. This product is indexed under FDA Product Code / Category Classification IRT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TheraFace Hot & Cold Rings Black
Product Code / EMDN: IRT
Device Name
Database Sync Date: 2026-08-09 09:17:03

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 TheraFace?

The registered manufacturer of record for TheraFace is Therabody, Inc..

What is the Primary UDI-DI identifier for TheraFace?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TheraFace Hot & Cold Rings Black.

What classification code is assigned to this device?

This device is registered under product classification code IRT.

Similar Classification Devices (IRT)

Other Devices by Therabody, Inc.

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