GUDIDData
eudamed_udi Primary ID: D-808166QS

Unspecified Brand (UDI D-808166QS)

Manufactured by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID D-808166QS

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 808166) is a medical device manufactured by Shenzhen Kang Sheng Bao Bio-Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160704 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
808166
Product Code / EMDN
W0102160704
Device Name
NT-proBNP Rapid Detect
Database Sync Date
2026-08-09 16:44:48

Full Regulatory Attributes

πŸ”’ 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 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-808166QS.

What classification code is assigned to this device?

This device is registered under product classification code W0102160704.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint