Patient monitoring system module, pulse oximetry - UK MHRA Medical Device Registration
Patient monitoring system module, pulse oximetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99022. The device is manufactured by Respironics Inc from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.
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Device Type
General Medical Device
Devices
Patient monitoring system module, pulse oximetry
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Jul 16, 2024
Relationship Type
Address
Ascent 1 Farnborough Aerospace Centre
Farnborough, Hampshire, England, United Kingdom
Postcode: GU14 6XW
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