eudamed_udi Primary ID: D-DCO-803N7

COC Rapid Test (UDI D-DCO-803N7)

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 COC Rapid Test (Model/Catalog Number: DCO-803) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160506 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DCO-803
Product Code / EMDN: W0102160506
Device Name: COC Rapid Test
Database Sync Date: 2026-08-09 18:34:15

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 COC Rapid Test?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-DCO-803N7.

What classification code is assigned to this device?

This device is registered under product classification code W0102160506.

Similar Classification Devices (W0102160506)

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

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