KEYU Feces Analyzer (UDI 06974735360958)
Manufactured by Zhuhai Keyu Biological Engineering Co., Ltd
Device Regulatory Overview
The KEYU Feces Analyzer (Model/Catalog Number: KU-F10) is a medical device manufactured by Zhuhai Keyu Biological Engineering Co., Ltd. This product is indexed under FDA Product Code / Category Classification W02010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KU-F10
- Product Code / EMDN
- W02010199
- Device Name
- Feces Analyzer
- Database Sync Date
- 2026-08-09 16:29:22
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 KEYU Feces Analyzer?
The registered manufacturer of record for KEYU Feces Analyzer is Zhuhai Keyu Biological Engineering Co., Ltd.
What is the Primary UDI-DI identifier for KEYU Feces Analyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974735360958.
What classification code is assigned to this device?
This device is registered under product classification code W02010199.
Similar Classification Devices (W02010199)
Other Devices by Zhuhai Keyu Biological Engineering Co., Ltd
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