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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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MX750/850 — 2 UDI-DI variants, MDR

MD Atlas
Philips Medizin Systeme Böblingen GmbH

Data from EUDAMED, last updated May 23, 2026

MX750/850

0884838BM591TG

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Philips Medizin Systeme Böblingen GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 0884838BM591TG
Device name: MX750/850
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Philips Medizin Systeme Böblingen GmbH
SRN: DE-MF-000006026
Country: Germany
Email: eudamed@philips.com
Phone: n/a

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JVA3DF8Z6YQ882J2ZE76SCQV

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

IntelliVue Patient Monitor MX75000884838083332
IntelliVue Patient Monitor MX85000884838070790