gudid
Primary ID: YF-HT2
HeadaTerm (UDI YF-HT2)
Manufactured by WAT Medical Technology Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HeadaTerm - Primary ID YF-HT2
Device Regulatory Overview
The HeadaTerm (Model/Catalog Number: YF-HT2) 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-HT2
- Product Code / EMDN
- PCC
- Device Name
- The TENS device-HeadaTerm 2 is indicated for the prophylactic treatment of episodic migraine in patients 18 years of age or older.
- 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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Get API Token Access ($49/mo)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-HT2.
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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