eufy (UDI T9201)
Manufactured by Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd.
Device Regulatory Overview
The eufy (Model/Catalog Number: T9201) is a medical device manufactured by Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T9201
- Product Code / EMDN
- DXN
- Device Name
- Database Sync Date
- 2026-08-09 09:05:28
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 eufy?
The registered manufacturer of record for eufy is Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd..
What is the Primary UDI-DI identifier for eufy?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is T9201.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Other Devices by Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd.
Programmatic Export
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JSON API Endpoint