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 160929. The device is manufactured by Onera B.V. from Netherlands, classified as General Medical Device. The authorized representative in the UK is MedEnvoy UK Limited.

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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Polysomnography analyser

MHRA Device ID: 160929•Ref: 160929

Device Type

General Medical Device

Devices

Polysomnography analyser

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 24, 2023

Manufacturer Information

Name

Onera B.V.

Address

Torenallee 42-54

Eindhoven, Netherlands

Created Date

Nov 17, 2022

Authorized Representative

Name

MedEnvoy UK Limited

Relationship Type

UK Responsible Person

Address

85 Great Portland Street First Floor

London, England, United Kingdom

Postcode: W1W 7LT

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Polysomnography analyser - UK MHRA Medical Device Registration

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