Unspecified Brand (UDI D-811030NS)
Manufactured by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 811030) is a medical device manufactured by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W01021699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 811030
- Product Code / EMDN
- W01021699
- Device Name
- FA/VB12/Fer Combined Test
- Database Sync Date
- 2026-08-09 16:45:04
Full Regulatory Attributes
๐ Token Gated
{
"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 Shenzhen Kang Sheng Bao Bio-Technology 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 D-811030NS.
What classification code is assigned to this device?
This device is registered under product classification code W01021699.
Similar Classification Devices (W01021699)
Other Devices by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.
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