eudamed_udi Primary ID: 06958982140754

One Step Methadone (MTD) Saliva Test (UDI 06958982140754)

Manufactured by Abiores Technology (Beijing) Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The One Step Methadone (MTD) Saliva Test (Model/Catalog Number: AD10-S20) is a medical device manufactured by Abiores Technology (Beijing) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AD10-S20
Product Code / EMDN: W0102160599
Device Name: One Step Methadone (MTD) Saliva Test
Database Sync Date: 2026-08-09 17:04:52

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 One Step Methadone (MTD) Saliva Test?

The registered manufacturer of record for One Step Methadone (MTD) Saliva Test is Abiores Technology (Beijing) Co.,Ltd..

What is the Primary UDI-DI identifier for One Step Methadone (MTD) Saliva Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140754.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Similar Classification Devices (W0102160599)

Other Devices by Abiores Technology (Beijing) Co.,Ltd.

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