GUDIDData
eudamed_udi Primary ID: 06975102441003

Unspecified Brand (UDI 06975102441003)

Manufactured by Jiangsu Qitian Gene biotechnology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06975102441003

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: F06004A-48) is a medical device manufactured by Jiangsu Qitian Gene biotechnology 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
F06004A-48
Product Code / EMDN
W0105900102
Device Name
Schistosoma Haematobium Nucleic Acid Detection Kit(Fluorescent RAA)
Database Sync Date
2026-08-09 16:46:16

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Jiangsu Qitian Gene biotechnology 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 06975102441003.

What classification code is assigned to this device?

This device is registered under product classification code W0105900102.

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