Pure Global

Bioelectrical signal analysis software - UK MHRA Medical Device Registration

Bioelectrical signal analysis software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 170320. The device is manufactured by Kvikna Medical ehf from Iceland, classified as General Medical Device. The authorized representative in the UK is PMF Consultants 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.

Free Database
Powered by Pure Global AI
MHRA Registered
General Medical Device
๐Ÿ‡ฌ๐Ÿ‡ง
Bioelectrical signal analysis software
MHRA Device ID: 170320โ€ขRef: 170320

Device Type

General Medical Device

Devices

Bioelectrical signal analysis software

Type

Class IIa

Date Registered

Apr 10, 2023

Last Updated

Oct 10, 2023

Manufacturer Information

Address

Lynghals 9

Reykjavik, Iceland

Created Date

Apr 10, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

10 Vail

Donaghadee, Co Down, Northern Ireland, United Kingdom

Postcode: BT21 0QL

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing