eudamed_udi Primary ID: 06952999405653

Unspecified Brand (UDI 06952999405653)

Manufactured by Abon Biopharm(Hangzhou) Co., Ltd

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 Abon Biopharm(Hangzhou) 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: ABON™ Urine Test Drug Screen Cassette
Database Sync Date: 2026-08-09 18:24:51

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 Abon Biopharm(Hangzhou) Co., Ltd.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06952999405653.

What classification code is assigned to this device?

This device is registered under product classification code W0102160506.

Similar Classification Devices (W0102160506)

Other Devices by Abon Biopharm(Hangzhou) Co., Ltd

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