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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 100837. The device is manufactured by Perimed AB from Sweden, classified as General Medical Device. 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.

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General Medical Device
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Laser Doppler blood flowmeter
MHRA Device ID: 100837•Ref: 100837

Device Type

General Medical Device

Devices

Laser Doppler blood flowmeter

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 4, 2024

Manufacturer Information

Address

Datavägen 9A

Järfälla, Sweden

Created Date

Aug 30, 2021

Authorized Representative

Relationship Type

UK Responsible Person

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

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Type: General Medical Device

Registered: Nov 26, 2024

Laser Doppler blood flowmeter

Type: General Medical Device

Registered: Nov 26, 2024

Laser Doppler blood flowmeter

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Registered: Nov 26, 2024

Laser Doppler blood flowmeter

Type: General Medical Device

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Laser Doppler blood flowmeter

Type: System or Procedure Pack

Registered: Nov 26, 2024

Laser Doppler blood flowmeter

Type: System or Procedure Pack

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Laser Doppler blood flowmeter

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