GUDIDData
eudamed_udi Primary ID: 06973342006303

Pathogen DNA/RNA Extraction Kit (Magnetic Bead Method) (UDI 06973342006303)

Manufactured by Jiangsu Bioperfectus Technologies Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pathogen DNA/RNA Extraction Kit (Magnetic Bead Method) - Primary ID 06973342006303

Device Regulatory Overview

The Pathogen DNA/RNA Extraction Kit (Magnetic Bead Method) (Model/Catalog Number: SDK60120-48T(8*6)) is a medical device manufactured by Jiangsu Bioperfectus Technologies 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
SDK60120-48T(8*6)
Product Code / EMDN
W0105900101
Device Name
Pathogen DNA/RNA Extraction Kit (Magnetic Bead Method)
Database Sync Date
2026-08-09 16:29:12

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 Pathogen DNA/RNA Extraction Kit (Magnetic Bead Method)?

The registered manufacturer of record for Pathogen DNA/RNA Extraction Kit (Magnetic Bead Method) is Jiangsu Bioperfectus Technologies Co., Ltd..

What is the Primary UDI-DI identifier for Pathogen DNA/RNA Extraction Kit (Magnetic Bead Method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973342006303.

What classification code is assigned to this device?

This device is registered under product classification code W0105900101.

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