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Mx40 - Wlan

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 865352Model MX40 Patient Wearable Monitor

by Philips Medical Systems

Identity

Trade Name
MX40 - WLAN EUDAMED
IntelliVue MX40 WLAN FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
MX40 Patient Wearable Monitor EUDAMED
IntelliVue MX40 Patient Worn Monitor operating on Hospital-supplied 802.11 a/b/g/n WLAN for communication to the Philips IntelliVue Information Center iX FDA UDI
Model / Reference
MX40 Patient Wearable Monitor EUDAMED
865352 EUDAMED
MX40 - WLAN FDA UDI
Description
IntelliVue MX40 Patient Worn Monitor operating on Hospital-supplied 802.11 a/b/g/n WLAN for communication to the Philips IntelliVue Information Center iX FDA UDI

Identifiers

Catalog Number
865352 FDA UDI
Primary DI / UDI-DI
00884838030350 EUDAMEDFDA UDI
Basic UDI-DI
B-00884838030350 EUDAMED
FDA Product Code
MHX FDA UDI
EMDN Code
Z12050803 ELECTROCARDIOGRAPH TELEMETRY SYSTEM TRANSMITTERS EUDAMED
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Mx40 - Wlan by Philips Medical Systems — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000002321
Authorised Representative
Philips Medizin Systeme Böblingen GmbH DE-AR-000006030

Sources (2)

  • EUDAMED 327a0c95-7ac6-48fb-8d2f-4faa367568b7 61 fields · synced Jul 8, 2026
  • FDA UDI d3afb4e4-4622-4509-9ed2-38aa9ac46123 36 fields · synced May 29, 2026