GUDIDData
eudamed_udi Primary ID: 06903053028936

N-terminal pro B-type natriuretic peptide (CLIA) (UDI 06903053028936)

Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N-terminal pro B-type natriuretic peptide (CLIA) - Primary ID 06903053028936

Device Regulatory Overview

The N-terminal pro B-type natriuretic peptide (CLIA) (Model/Catalog Number: 105-027045-00) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01021301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
105-027045-00
Product Code / EMDN
W01021301
Device Name
N-terminal pro B-type natriuretic peptide (CLIA)、NT-proBNP calibrators、NT-proBNP Control
Database Sync Date
2026-08-09 16:51:10

Full Regulatory Attributes

🔒 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 N-terminal pro B-type natriuretic peptide (CLIA)?

The registered manufacturer of record for N-terminal pro B-type natriuretic peptide (CLIA) is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..

What is the Primary UDI-DI identifier for N-terminal pro B-type natriuretic peptide (CLIA)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06903053028936.

What classification code is assigned to this device?

This device is registered under product classification code W01021301.

Similar Classification Devices (W01021301)

Other Devices by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

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