eudamed_udi
Primary ID: 06975447582119
Unspecified Brand (UDI 06975447582119)
Manufactured by Igenesis(Shanghai)Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06975447582119
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 106-0056-01) is a medical device manufactured by Igenesis(Shanghai)Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0105010703 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 106-0056-01
- Product Code / EMDN
- W0105010703
- Device Name
- Diagnostic Kit for Mycobacterium Tuberculosis(MTB) complex DNA and Rifampicin resistance Mycobacterium tuberculosis(PCR-Fluorescence)
- Database Sync Date
- 2026-08-09 16:30:29
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 Igenesis(Shanghai)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 06975447582119.
What classification code is assigned to this device?
This device is registered under product classification code W0105010703.
Similar Classification Devices (W0105010703)
Other Devices by Igenesis(Shanghai)Co.,Ltd.
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