← Back to catalogue

PHILIPS IntelliVue MP2 Military

FDA UDI

Class II (US FDA UDI)

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
PHILIPS IntelliVue MP2 Military FDA UDI
Generic Name
Multiple vital physiological parameter monitoring system, clinical FDA UDI
Model / Reference
867059 FDA UDI

Identifiers

Catalog Number
867059 FDA UDI
Primary DI / UDI-DI
00884838064904 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Multiple vital physiological parameter monitoring system, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

PHILIPS IntelliVue MP2 Military by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI cdb93db0-0c0c-43ae-b490-6dbfda918f1b 35 fields · synced May 30, 2026