KEYU Urine Sediment Analyzer (UDI 06974735360033)
Manufactured by Zhuhai Keyu Biological Engineering Co., Ltd
Device Regulatory Overview
The KEYU Urine Sediment Analyzer (Model/Catalog Number: KU-600) is a medical device manufactured by Zhuhai Keyu Biological Engineering Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0201010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KU-600
- Product Code / EMDN
- W0201010202
- Device Name
- Urine Sediment Analyzer
- Database Sync Date
- 2026-08-09 16:59:44
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 Urine Sediment Analyzer?
The registered manufacturer of record for KEYU Urine Sediment Analyzer is Zhuhai Keyu Biological Engineering Co., Ltd.
What is the Primary UDI-DI identifier for KEYU Urine Sediment Analyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974735360033.
What classification code is assigned to this device?
This device is registered under product classification code W0201010202.
Similar Classification Devices (W0201010202)
Other Devices by Zhuhai Keyu Biological Engineering Co., Ltd
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