Unspecified Brand (UDI 06971760720023)
Manufactured by QINGDAO HUAREN MEDICAL PRODUCT CO.,LTD.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 10 tests/kit) is a medical device manufactured by QINGDAO HUAREN MEDICAL PRODUCT CO.,LTD.. This product is indexed under FDA Product Code / Category Classification W0105900102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10 tests/kit
- Product Code / EMDN
- W0105900102
- Device Name
- Detection Kit for Monkeypox Virus DNA (PCR-Fluorescence Probing)
- Database Sync Date
- 2026-08-09 16:50:54
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is QINGDAO HUAREN MEDICAL PRODUCT CO.,LTD..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971760720023.
What classification code is assigned to this device?
This device is registered under product classification code W0105900102.
Similar Classification Devices (W0105900102)
Other Devices by QINGDAO HUAREN MEDICAL PRODUCT CO.,LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint