eudamed_udi Primary ID: 06958982140471

(KET) Ketamine Test (UDI 06958982140471)

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 (KET) Ketamine Test (Model/Catalog Number: AD03-11) 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: AD03-11
Product Code / EMDN: W0102160599
Device Name: (KET) Ketamine Test
Database Sync Date: 2026-08-09 18:07:46

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 (KET) Ketamine Test?

The registered manufacturer of record for (KET) Ketamine Test is Abiores Technology (Beijing) Co.,Ltd..

What is the Primary UDI-DI identifier for (KET) Ketamine Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140471.

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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