Laser Doppler blood flowmeter - UK MHRA Medical Device Registration
Laser Doppler blood flowmeter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 167482. The device is manufactured by Perimed AB from Sweden, classified as System or Procedure Pack. The authorized representative in the UK is QAdvis 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
System or Procedure Pack
Devices
Laser Doppler blood flowmeter
Type
System or Procedure Pack
Date Registered
Nov 26, 2024
Last Updated
Jul 4, 2024
Name
QAdvis UK LtdRelationship Type
Address
55-66 Frederick Street
Edinburgh, EH2 1LS, Scotland, United Kingdom
Postcode: EH2 1LS
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Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: System or Procedure Pack
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: System or Procedure Pack
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: System or Procedure Pack
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
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