C-REACTIVE PROTEIN REAGENT KIT（LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY） (UDI 06942202246760)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The C-REACTIVE PROTEIN REAGENT KIT（LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY） (Model/Catalog Number: 232021602032) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01021109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 232021602032
- Product Code / EMDN
- W01021109
- Device Name
- C-REACTIVE PROTEIN REAGENT KIT（LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY）
- Database Sync Date
- 2026-08-09 16:47:03
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 C-REACTIVE PROTEIN REAGENT KIT（LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY）?
The registered manufacturer of record for C-REACTIVE PROTEIN REAGENT KIT（LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY） is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for C-REACTIVE PROTEIN REAGENT KIT（LATEX ENHANCED IMMUNOTURBIDIMETRIC ASSAY）?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202246760.
What classification code is assigned to this device?
This device is registered under product classification code W01021109.
Similar Classification Devices (W01021109)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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