eudamed_udi Primary ID: 06942598225523

Pregabalin(PGB) Rapid Test (UDI 06942598225523)

Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pregabalin(PGB) Rapid Test (Model/Catalog Number: DPG-N111B-50) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DPG-N111B-50
Product Code / EMDN: W0102160511
Device Name: Pregabalin(PGB) Rapid Test
Database Sync Date: 2026-08-09 16:29:41

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Pregabalin(PGB) Rapid Test?

The registered manufacturer of record for Pregabalin(PGB) Rapid Test is Hangzhou Alltest Biotech.Co.,Ltd..

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942598225523.

What classification code is assigned to this device?

This device is registered under product classification code W0102160511.

Similar Classification Devices (W0102160511)

Other Devices by Hangzhou Alltest Biotech.Co.,Ltd.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint