eudamed_udi Primary ID: 06974081870248

Nucleic Acid Extractor (UDI 06974081870248)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Nucleic Acid Extractor (Model/Catalog Number: 043) is a medical device manufactured by SINGUWAY BIOTECH INC.. This product is indexed under FDA Product Code / Category Classification W02069099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 043
Product Code / EMDN: W02069099
Device Name: Nucleic Acid Extractor
Database Sync Date: 2026-08-09 16:45:43

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 Nucleic Acid Extractor?

The registered manufacturer of record for Nucleic Acid Extractor is SINGUWAY BIOTECH INC..

What is the Primary UDI-DI identifier for Nucleic Acid Extractor?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974081870248.

What classification code is assigned to this device?

This device is registered under product classification code W02069099.

Similar Classification Devices (W02069099)

Other Devices by SINGUWAY BIOTECH INC.

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