eudamed_udi Primary ID: 06958982140884

(PGB) Pregabalin Test (UDI 06958982140884)

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 (PGB) Pregabalin Test (Model/Catalog Number: AD38-11) 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: AD38-11
Product Code / EMDN: W0102160599
Device Name: (PGB) Pregabalin Test
Database Sync Date: 2026-08-09 16:45:46

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 (PGB) Pregabalin Test?

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

What is the Primary UDI-DI identifier for (PGB) Pregabalin Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140884.

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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