Polysomnography analyser - UK MHRA Medical Device Registration
Polysomnography analyser is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99008. 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.
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.
Device Type
General Medical Device
Devices
Polysomnography analyser
Type
Class IIa
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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