gudid Primary ID: YF-HT-W1

HeadaTerm (UDI YF-HT-W1)

Manufactured by WAT Medical Technology Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HeadaTerm (Model/Catalog Number: YF-HT-W1) is a medical device manufactured by WAT Medical Technology Inc.. This product is indexed under FDA Product Code / Category Classification PCC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: YF-HT-W1
Product Code / EMDN: PCC
Device Name: TENS device-HeadaTerm offers a drug-free scheme, which introduces electric impulses to act on the supraorbital nerve and supratrochlear nerve, the very nerves that transmit migraine pain, to treat and prevent migraine headaches. TENS deviceHeadaTerm enables an electronic feedback mechanism to adjust the electrical impulses to the specific requirements of the individual user for personalized efficacy and comfort.The device could adhere to patients forehead with conductive paste, the current passing through the electrodes and release current stimulate the nerve underneath patients' forehead skin; the stimulation would alleviate migraine headaches, and during ramping up, patients could choose comfortable intensity level by pressing the host key to lock up the current voltage, and the patient contact material is biocompatibility safe. The conductive paste could be replaced once the paste lost its adhesiveness and patients are recommended to replace the conductive paste after 7 times of treatment uses.
Database Sync Date: 2026-08-09 09:06:41

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 HeadaTerm?

The registered manufacturer of record for HeadaTerm is WAT Medical Technology Inc..

What is the Primary UDI-DI identifier for HeadaTerm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is YF-HT-W1.

What classification code is assigned to this device?

This device is registered under product classification code PCC.

Similar Classification Devices (PCC)

Other Devices by WAT Medical Technology Inc.

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