FDA device listing

867036, IntelliVue Multi-Measurement Module MMX

FDA device listing 1077472669 · Philips Medical Systems International BV

Key facts

Proprietary names 867036, IntelliVue Multi-Measurement Module MMX
Owner/operator Philips Medical Systems International BV
Owner/operator number 1217116
Premarket submissions K181831
Product codes DRQ, DSI, DSJ, DSK, DXG, DXN, MHX, MLD
Device names DRQ - Amplifier And Signal Conditioner, Transducer Signal, DSI - Detector And Alarm, Arrhythmia, DSJ - Alarm, Blood-Pressure, DSK - Computer, Blood-Pressure, DXG - Computer, Diagnostic, Pre-Programmed, Single-Function, DXN - System, Measurement, Blood-Pressure, Non-Invasive, MHX - Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms), MLD - Monitor, St Segment With Alarm
Device class Class II
Classification regulations (21 CFR) 870.1025, 870.1100, 870.1110, 870.1130, 870.1435, 870.2060
Review panels Cardiovascular
Registered establishments Philips Electronics Ltd, Philips Medizin Systeme Boeblingen GmbH, Philips North America LLC
Establishment registrations 9610816, 3000126629, 3012528160, 3016701404
FEI numbers 3000126629, 3002807167, 3012528160, 3016701404
Establishment operations Complaint File Establishment, Manufacturer, Contract Manufacturer, Foreign Exporter
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings