LOW DENSITY LIPOPROTEIN CHOLESTEROL REAGENT KIT（DIRECT METHOD） (UDI 06942202213472)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The LOW DENSITY LIPOPROTEIN CHOLESTEROL REAGENT KIT（DIRECT METHOD） (Model/Catalog Number: 3023259) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010221 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3023259
- Product Code / EMDN
- W01010221
- Device Name
- LOW DENSITY LIPOPROTEIN CHOLESTEROL REAGENT KIT（DIRECT METHOD）
- Database Sync Date
- 2026-08-09 17:37:31
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 LOW DENSITY LIPOPROTEIN CHOLESTEROL REAGENT KIT（DIRECT METHOD）?
The registered manufacturer of record for LOW DENSITY LIPOPROTEIN CHOLESTEROL REAGENT KIT（DIRECT METHOD） is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for LOW DENSITY LIPOPROTEIN CHOLESTEROL REAGENT KIT（DIRECT METHOD）?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202213472.
What classification code is assigned to this device?
This device is registered under product classification code W01010221.
Similar Classification Devices (W01010221)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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