eudamed_udi Primary ID: 06975068490329

Progesterone（Prog）Rapid Quantitative Test（Fluorescence Immunoassay） (UDI 06975068490329)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Progesterone（Prog）Rapid Quantitative Test（Fluorescence Immunoassay） (Model/Catalog Number: CP070.B1) is a medical device manufactured by WWHS Biotech.Inc. This product is indexed under FDA Product Code / Category Classification W0102030202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CP070.B1
Product Code / EMDN: W0102030202
Device Name: Progesterone（Prog）Rapid Quantitative Test（Fluorescence Immunoassay）
Database Sync Date: 2026-08-09 18:36:58

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 Progesterone（Prog）Rapid Quantitative Test（Fluorescence Immunoassay）?

The registered manufacturer of record for Progesterone（Prog）Rapid Quantitative Test（Fluorescence Immunoassay） is WWHS Biotech.Inc.

What is the Primary UDI-DI identifier for Progesterone（Prog）Rapid Quantitative Test（Fluorescence Immunoassay）?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975068490329.

What classification code is assigned to this device?

This device is registered under product classification code W0102030202.

Similar Classification Devices (W0102030202)

Other Devices by WWHS Biotech.Inc

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