Lipoprotein-Associated Phospholipase A2 Reagent Kit (Latex Immunoturbidimetric Assay) (UDI 06942202227882)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The Lipoprotein-Associated Phospholipase A2 Reagent Kit (Latex Immunoturbidimetric Assay) (Model/Catalog Number: 3025047) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01021312 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3025047
- Product Code / EMDN
- W01021312
- Device Name
- Lipoprotein-Associated Phospholipase A2 Reagent Kit (Latex Immunoturbidimetric Assay)
- Database Sync Date
- 2026-08-09 18:16:41
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 Lipoprotein-Associated Phospholipase A2 Reagent Kit (Latex Immunoturbidimetric Assay)?
The registered manufacturer of record for Lipoprotein-Associated Phospholipase A2 Reagent Kit (Latex Immunoturbidimetric Assay) is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for Lipoprotein-Associated Phospholipase A2 Reagent Kit (Latex Immunoturbidimetric Assay)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202227882.
What classification code is assigned to this device?
This device is registered under product classification code W01021312.
Similar Classification Devices (W01021312)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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