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IntelliVue X3

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 867030

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
IntelliVue X3 EUDAMED
IntelliVue Multi-Measurement Module X3 FDA UDI
Generic Name
Multiple vital physiological parameter monitoring system, clinical FDA UDI
Device Name
X3/MX100 EUDAMED
IntelliVue Multi-Measurement Module X3, compact, battery operated patient monitor and multi-measurement module. FDA UDI
Model / Reference
867030 EUDAMED
IntelliVue X3 FDA UDI
Description
IntelliVue Multi-Measurement Module X3, compact, battery operated patient monitor and multi-measurement module. FDA UDI

Identifiers

Catalog Number
867030 FDA UDI
Primary DI / UDI-DI
00884838082588 EUDAMEDFDA UDI
Basic UDI-DI
0884838BM537TA EUDAMED
Direct Marketing DI
00884838082588 EUDAMED
FDA Product Code
MHX FDA UDI
EMDN Code
Z1203020299 MULTI–PARAMETER MONITORS - OTHER EUDAMED
GMDN Term
Multiple vital physiological parameter monitoring system, clinical 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

IntelliVue X3 by Philips Medizin Systeme Böblingen GmbH — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Philips Medizin Systeme Böblingen GmbH
EUDAMED SRN
DE-MF-000006026

Sources (2)

  • EUDAMED 6d6f6657-bf26-4a2b-86f6-f49313142a38 61 fields · synced May 31, 2026
  • FDA UDI 4c36a06e-cf23-420b-842b-47aeb802f766 36 fields · synced May 29, 2026