Haemodynamic monitoring system application software - UK MHRA Medical Device Registration

Haemodynamic monitoring system application software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91757. The device is manufactured by Philips Medical Systems Nederland B.V. from Netherlands, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Haemodynamic monitoring system application software

MHRA Device ID: 91757•Ref: 91757

Device Type

General Medical Device

Devices

Haemodynamic monitoring system application software

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

May 14, 2024

Manufacturer Information

Name

Philips Medical Systems Nederland B.V.

Address

IGT-S Veenpluis 6

Best, Netherlands

Created Date

Aug 2, 2021

Authorized Representative

Name

Philips Electronics UK Ltd

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

DJ Fang

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Haemodynamic monitoring system application software - UK MHRA Medical Device Registration

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DJ Fang

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