← Back to catalogue

MR Patient Care Portal Remote Display # 5000

FDA UDI

Class II (US FDA UDI)

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
MR Patient Care Portal Remote Display # 5000 FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
MR Patient Care Portal 5000 FDA UDI
Model / Reference
MR Patient Care Portal 5000 FDA UDI
Description
MR Patient Care Portal 5000 FDA UDI

Identifiers

Catalog Number
866162 FDA UDI
Primary DI / UDI-DI
00884838124066 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 FDA UDI
Commercial Distribution
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

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

Category: General-purpose multi-parameter bedside monitor

MR Patient Care Portal Remote Display # 5000 by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

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

Manufacturer
Philips Medizin Systeme Böblingen GmbH

Sources (1)

  • FDA UDI 1f4d453c-a777-4ea6-ba5f-703b7b7fa148 35 fields · synced Jun 1, 2026