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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 99191. The device is manufactured by Nox Medical from Iceland, classified as System or Procedure Pack. The authorized representative in the UK is Qserve Group 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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System or Procedure Pack
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Polysomnography analyser
MHRA Device ID: 99191โ€ขRef: 99191

Device Type

System or Procedure Pack

Devices

Polysomnography analyser

Type

System or Procedure Pack

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Address

Katrinartuni 2,

Reykjavik, Iceland

Created Date

Aug 26, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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