α2-macroglobulin Reagent Kit (Immunoturbidimetric Assay) (UDI 06942202238567)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The α2-macroglobulin Reagent Kit (Immunoturbidimetric Assay) (Model/Catalog Number: 3011374) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W0102019003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3011374
- Product Code / EMDN
- W0102019003
- Device Name
- α2-macroglobulin Reagent Kit (Immunoturbidimetric Assay)
- Database Sync Date
- 2026-08-09 16:47:15
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 α2-macroglobulin Reagent Kit (Immunoturbidimetric Assay)?
The registered manufacturer of record for α2-macroglobulin Reagent Kit (Immunoturbidimetric Assay) is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for α2-macroglobulin Reagent Kit (Immunoturbidimetric Assay)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202238567.
What classification code is assigned to this device?
This device is registered under product classification code W0102019003.
Similar Classification Devices (W0102019003)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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