eudamed_udi Primary ID: 06974912093914

POCBio Malaria Pf Rapid Test (UDI 06974912093914)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The POCBio Malaria Pf Rapid Test (Model/Catalog Number: LATT03-C50) is a medical device manufactured by Nexlab Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105090401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: LATT03-C50
Product Code / EMDN: W0105090401
Device Name: POCBio Malaria Pf Rapid Test
Database Sync Date: 2026-08-09 16:30:22

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 POCBio Malaria Pf Rapid Test?

The registered manufacturer of record for POCBio Malaria Pf Rapid Test is Nexlab Co., Ltd..

What is the Primary UDI-DI identifier for POCBio Malaria Pf Rapid Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974912093914.

What classification code is assigned to this device?

This device is registered under product classification code W0105090401.

Similar Classification Devices (W0105090401)

Other Devices by Nexlab Co., Ltd.

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