eudamed_udi Primary ID: 06936983142465

Multi- Drug Rapid Test (UDI 06936983142465)

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 Multi- Drug Rapid Test (Model/Catalog Number: DOA-N164-020) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DOA-N164-020
Product Code / EMDN: W0102160511
Device Name: Multi- Drug Rapid Test
Database Sync Date: 2026-08-09 16:29:21

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 Multi- Drug Rapid Test?

The registered manufacturer of record for Multi- Drug Rapid Test is Hangzhou Alltest Biotech.Co.,Ltd..

What is the Primary UDI-DI identifier for Multi- Drug Rapid Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936983142465.

What classification code is assigned to this device?

This device is registered under product classification code W0102160511.

Similar Classification Devices (W0102160511)

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

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