GUDIDData
eudamed_udi Primary ID: 06973342006013

Cell Nucleic Acid Extraction Kit (Magnetic Bead Method) (UDI 06973342006013)

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 Cell Nucleic Acid Extraction Kit (Magnetic Bead Method) - Primary ID 06973342006013

Device Regulatory Overview

The Cell Nucleic Acid Extraction Kit (Magnetic Bead Method) (Model/Catalog Number: SDK80125A-48T) 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
SDK80125A-48T
Product Code / EMDN
W0105900101
Device Name
Cell Nucleic Acid Extraction Kit (Magnetic Bead Method)
Database Sync Date
2026-08-09 16:50:55

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 Cell Nucleic Acid Extraction Kit (Magnetic Bead Method)?

The registered manufacturer of record for Cell Nucleic Acid Extraction Kit (Magnetic Bead Method) is Jiangsu Bioperfectus Technologies Co., Ltd..

What is the Primary UDI-DI identifier for Cell Nucleic Acid Extraction Kit (Magnetic Bead Method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973342006013.

What classification code is assigned to this device?

This device is registered under product classification code W0105900101.

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