GUDIDData
eudamed_udi Primary ID: 06974969980694

Nucleic Acid Extraction Kit (UDI 06974969980694)

Manufactured by Biobase Diagnostic Technology (Shandong) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nucleic Acid Extraction Kit - Primary ID 06974969980694

Device Regulatory Overview

The Nucleic Acid Extraction Kit (Model/Catalog Number: ZD001) is a medical device manufactured by Biobase Diagnostic Technology (Shandong) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105900101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ZD001
Product Code / EMDN
W0105900101
Device Name
Nucleic Acid Extraction Kit
Database Sync Date
2026-08-09 16:29:59

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Kit?

The registered manufacturer of record for Nucleic Acid Extraction Kit is Biobase Diagnostic Technology (Shandong) Co., Ltd..

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974969980694.

What classification code is assigned to this device?

This device is registered under product classification code W0105900101.

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