gudid Primary ID: Nonin SpO2 Mortara+ST

Transmitter (UDI Nonin SpO2 Mortara+ST)

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

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Transmitter (Model/Catalog Number: Nonin SpO2 Mortara+ST) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification MSX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Nonin SpO2 Mortara+ST
Product Code / EMDN: MSX
Device Name
Database Sync Date: 2026-08-09 09:11:05

Full Regulatory Attributes

🔒 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 Transmitter?

The registered manufacturer of record for Transmitter is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..

What is the Primary UDI-DI identifier for Transmitter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Nonin SpO2 Mortara+ST.

What classification code is assigned to this device?

This device is registered under product classification code MSX.

Similar Classification Devices (MSX)

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

Programmatic Export

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

JSON API Endpoint