eudamed_udi Primary ID: D-IEH-602NV

Entamoeba histolytica Rapid Test Cassette (UDI D-IEH-602NV)

Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Entamoeba histolytica Rapid Test Cassette (Model/Catalog Number: IEH-602) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0105050201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: IEH-602
Product Code / EMDN: W0105050201
Device Name: Entamoeba histolytica Rapid Test Cassette
Database Sync Date: 2026-08-09 17:04:13

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 Entamoeba histolytica Rapid Test Cassette?

The registered manufacturer of record for Entamoeba histolytica Rapid Test Cassette is Hangzhou Alltest Biotech.Co.,Ltd..

What is the Primary UDI-DI identifier for Entamoeba histolytica Rapid Test Cassette?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-IEH-602NV.

What classification code is assigned to this device?

This device is registered under product classification code W0105050201.

Similar Classification Devices (W0105050201)

Other Devices by Hangzhou Alltest Biotech.Co.,Ltd.

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