Unspecified Brand (UDI D-808128-1B8)
Manufactured by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 808128-1) is a medical device manufactured by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0105099099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 808128-1
- Product Code / EMDN
- W0105099099
- Device Name
- Rotavirus & Adenovirus Rapid Test
- Database Sync Date
- 2026-08-09 16:58:13
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 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-808128-1B8.
What classification code is assigned to this device?
This device is registered under product classification code W0105099099.
Similar Classification Devices (W0105099099)
Other Devices by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.
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