Laser speckle blood flowmeter - UK MHRA Medical Device Registration
Laser speckle blood flowmeter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 167469. The device is manufactured by Perimed AB from Sweden, classified as General Medical Device. The authorized representative in the UK is QAdvis UK Ltd.
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Device Type
General Medical Device
Devices
Laser speckle blood flowmeter
Type
Class IIa
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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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
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Registered: Nov 26, 2024
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Registered: Nov 26, 2024
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Type: System or Procedure Pack
Registered: Nov 26, 2024
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Type: System or Procedure Pack
Registered: Nov 26, 2024
Laser Doppler blood flowmeter
Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Manufacturer: Perimed AB
Laser Doppler blood flowmeter
Type: General Medical Device
Manufacturer: Perimed AB
Laser Doppler blood flowmeter
Type: General Medical Device
Manufacturer: Perimed AB
Laser Doppler blood flowmeter
Type: General Medical Device
Manufacturer: Perimed AB
Laser Doppler blood flowmeter
Type: General Medical Device
Manufacturer: Perimed AB
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Type: General Medical Device
Manufacturer: Perimed AB
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Type: In Vitro Diagnostic Device
Manufacturer: CareDx AB