GUDIDData
eudamed_udi Primary ID: 00884838055025

Wireless SpO2 3.0 Module (Networks 1-5) (UDI 00884838055025)

Manufactured by Invivo, a division of Philips Medical Systems

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wireless SpO2 3.0 Module (Networks 1-5) - Primary ID 00884838055025

Device Regulatory Overview

The Wireless SpO2 3.0 Module (Networks 1-5) (Model/Catalog Number: 989803192771) is a medical device manufactured by Invivo, a division of Philips Medical Systems. This product is indexed under FDA Product Code / Category Classification Z1203020299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
989803192771
Product Code / EMDN
Z1203020299
Device Name
Expression MR400 MRI Patient Monitor Sys
Database Sync Date
2026-08-09 16:29:13

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 Wireless SpO2 3.0 Module (Networks 1-5)?

The registered manufacturer of record for Wireless SpO2 3.0 Module (Networks 1-5) is Invivo, a division of Philips Medical Systems.

What is the Primary UDI-DI identifier for Wireless SpO2 3.0 Module (Networks 1-5)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838055025.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020299.

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