Nucleic Acid Extraction Kit (UDI 06974969980694)
Manufactured by Biobase Diagnostic Technology (Shandong) Co., Ltd.
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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)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.
Similar Classification Devices (W0105900101)
Other Devices by Biobase Diagnostic Technology (Shandong) Co., Ltd.
- → Testosterone(T)Detection Kit(Magnetic Solid Phase Chemiluminescent Immunoassay)
- → Disposable Virus Sampling Tube
- → Cortisol Detection Kit(Magnetic Solid Phase Chemiluminescent Immunoassay)
- → Pro-gastrin-releasing Peptide(proGRP)Detection Kit(Magnetic Solid Phase Chemiluminescent Immunoassay )
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint