eudamed_udi Primary ID: 06975068490503

Diagnostic Kit for Lipoprotein-Associated Phospholipase A2（Immunochromatographic assay） (UDI 06975068490503)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Diagnostic Kit for Lipoprotein-Associated Phospholipase A2（Immunochromatographic assay） (Model/Catalog Number: CP006.B1) is a medical device manufactured by WWHS Biotech.Inc. This product is indexed under FDA Product Code / Category Classification W01021312 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CP006.B1
Product Code / EMDN: W01021312
Device Name: Diagnostic Kit for Lipoprotein-Associated Phospholipase A2（Immunochromatographic assay）
Database Sync Date: 2026-08-09 18:32:51

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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Frequently Asked Questions

Who is the primary manufacturer of Diagnostic Kit for Lipoprotein-Associated Phospholipase A2（Immunochromatographic assay）?

The registered manufacturer of record for Diagnostic Kit for Lipoprotein-Associated Phospholipase A2（Immunochromatographic assay） is WWHS Biotech.Inc.

What is the Primary UDI-DI identifier for Diagnostic Kit for Lipoprotein-Associated Phospholipase A2（Immunochromatographic assay）?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975068490503.

What classification code is assigned to this device?

This device is registered under product classification code W01021312.

Similar Classification Devices (W01021312)

Other Devices by WWHS Biotech.Inc

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