eudamed_udi Primary ID: D-DCO-102M2

Unspecified Brand (UDI D-DCO-102M2)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: DCO-102) is a medical device manufactured by CITEST DIAGNOSTICS INC. 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: Cocaine (COC300) Rapid Test Cassette
Database Sync Date: 2026-08-09 17:37:43

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is CITEST DIAGNOSTICS INC.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-DCO-102M2.

What classification code is assigned to this device?

This device is registered under product classification code W0102160506.

Similar Classification Devices (W0102160506)

Other Devices by CITEST DIAGNOSTICS INC

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