GUDIDData
eudamed_udi Primary ID: 06974674891933

Nucleic Acid Extraction or Purification Kit (UDI 06974674891933)

Manufactured by Shenzhen Zijian Biotechnology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nucleic Acid Extraction or Purification Kit - Primary ID 06974674891933

Device Regulatory Overview

The Nucleic Acid Extraction or Purification Kit (Model/Catalog Number: 18-04-0019) is a medical device manufactured by Shenzhen Zijian Biotechnology 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
18-04-0019
Product Code / EMDN
W0105900101
Device Name
Nucleic Acid Extraction or Purification Kit
Database Sync Date
2026-08-09 16:29:39

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 or Purification Kit?

The registered manufacturer of record for Nucleic Acid Extraction or Purification Kit is Shenzhen Zijian Biotechnology Co., Ltd.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974674891933.

What classification code is assigned to this device?

This device is registered under product classification code W0105900101.

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