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IntelliVue MMX

by Philips Medizin Systeme Böblingen GmbH

Ref 867036Model MMX

Active European Union. Also listed in GUDID (US).

CE MDR CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number0884838BM587TR Basic UDI-DI 00884838086760UDI-DIDate24 Feb 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number0884838BM587TR Basic UDI-DI 00884838086760UDI-DIDate24 Feb 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00884838086760 UDI-DI Date19 Mar 2019ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD, CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
IntelliVue MMX EUDAMED
IntelliVue Multi-Measurement Module MMX GUDID
Generic Name
Patient monitoring system module, multifunction
Device Name
Mmx
Model / Ref / Catalog
MMX, 867036, IntelliVue MMX
Primary DI / UDI-DI
00884838086760
Basic UDI-DI
0884838BM587TR, B-00884838086760
Direct Marketing DI
00884838086760
FDA Product Code
MHX
EMDN Code
Z12030280 Vital signs monitoring instruments - hardware accessories
GMDN Term
Patient monitoring system module, multifunction
Device Class
Class IIb EUDAMED
Class II GUDID
Regulation Number
870.1025
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
MMX
867036
GUDID
IntelliVue MMX
Device ClassEUDAMED
Class IIb
GUDID
Class II

Manufacturer details

EUDAMED SRN
DE-MF-000006026

Related devices

Category: Electrical-only medical device connection cable, reusable

Other devices from Philips Medizin Systeme Böblingen GmbH

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Properties

  • Measuring Function
  • Prescription Use
  • Serial Number

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No