GUDIDData
eudamed_udi Primary ID: 06975529470082

Nucleic Acid Extraction Instrument (UDI 06975529470082)

Manufactured by Shenzhen Nucleus Biotechnology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nucleic Acid Extraction Instrument - Primary ID 06975529470082

Device Regulatory Overview

The Nucleic Acid Extraction Instrument (Model/Catalog Number: 966C0001) is a medical device manufactured by Shenzhen Nucleus Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W02069099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
966C0001
Product Code / EMDN
W02069099
Device Name
Nucleic Acid Extraction Instruments
Database Sync Date
2026-08-09 16:51:46

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 Nucleic Acid Extraction Instrument?

The registered manufacturer of record for Nucleic Acid Extraction Instrument is Shenzhen Nucleus Biotechnology Co., Ltd..

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975529470082.

What classification code is assigned to this device?

This device is registered under product classification code W02069099.

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