GUDIDData
eudamed_udi Primary ID: 06950996003827

NT-proBNP Quantitative Test Kit (Time-Resolved FIA) (UDI 06950996003827)

Manufactured by Zhejiang Orient Gene Biotech Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NT-proBNP Quantitative Test Kit (Time-Resolved FIA) - Primary ID 06950996003827

Device Regulatory Overview

The NT-proBNP Quantitative Test Kit (Time-Resolved FIA) (Model/Catalog Number: FDBNP-402a-DR10) is a medical device manufactured by Zhejiang Orient Gene Biotech 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
FDBNP-402a-DR10
Product Code / EMDN
W0102160704
Device Name
NT-proBNP Quantitative Test Kit (Time-Resolved FIA)
Database Sync Date
2026-08-09 16:29:58

Full Regulatory Attributes

πŸ”’ 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 NT-proBNP Quantitative Test Kit (Time-Resolved FIA)?

The registered manufacturer of record for NT-proBNP Quantitative Test Kit (Time-Resolved FIA) is Zhejiang Orient Gene Biotech Co., Ltd.

What is the Primary UDI-DI identifier for NT-proBNP Quantitative Test Kit (Time-Resolved FIA)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06950996003827.

What classification code is assigned to this device?

This device is registered under product classification code W0102160704.

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