LDL-Cholesterol Kit (Direct Method) (UDI 06944904024929)
Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Device Regulatory Overview
The LDL-Cholesterol Kit (Direct Method) (Model/Catalog Number: 105-000836-00) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics 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
- 105-000836-00
- Product Code / EMDN
- W01010221
- Device Name
- LDL-Cholesterol Kit (Direct Method)
- Database Sync Date
- 2026-08-09 16:48:49
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 LDL-Cholesterol Kit (Direct Method)?
The registered manufacturer of record for LDL-Cholesterol Kit (Direct Method) is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..
What is the Primary UDI-DI identifier for LDL-Cholesterol Kit (Direct Method)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944904024929.
What classification code is assigned to this device?
This device is registered under product classification code W01010221.
Similar Classification Devices (W01010221)
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