GUDIDData
eudamed_udi Primary ID: 06970277510578

COC Rapid Test Cassette (UDI 06970277510578)

Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COC Rapid Test Cassette - Primary ID 06970277510578

Device Regulatory Overview

The COC Rapid Test Cassette (Model/Catalog Number: DCO-102) 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-102
Product Code / EMDN
W0102160506
Device Name
COC Rapid Test Cassette
Database Sync Date
2026-08-09 16:29:02

Full Regulatory Attributes

๐Ÿ”’ Token Gated
{
    "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 Cassette?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970277510578.

What classification code is assigned to this device?

This device is registered under product classification code W0102160506.

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