eudamed_udi Primary ID: 06974912094256

Propoxyphene (PPX) Rapid Test (UDI 06974912094256)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Propoxyphene (PPX) Rapid Test (Model/Catalog Number: DUPPX-C50) is a medical device manufactured by Nexlab 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: DUPPX-C50
Product Code / EMDN: W0102160599
Device Name: Propoxyphene (PPX) Rapid Test
Database Sync Date: 2026-08-09 16:44:52

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 Propoxyphene (PPX) Rapid Test?

The registered manufacturer of record for Propoxyphene (PPX) Rapid Test is Nexlab Co., Ltd..

What is the Primary UDI-DI identifier for Propoxyphene (PPX) Rapid Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974912094256.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Similar Classification Devices (W0102160599)

Other Devices by Nexlab Co., Ltd.

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