Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Prolira B.V.

Address:

Padualaan 8

Utrecht

Utrecht 3584 CH

Netherlands

Authorised Representative/ UK Responsible Person
Name: Qarad UK Ltd.
Address:

8 Northumberland Ave

Westminster

London WC2N 5BY

England United Kingdom

Code/Term Type

Analytical scalp electrode single-use Analytical scalp electrode single-use Class I

Electroencephalographic monitoring system Electroencephalographic monitoring system Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Analytical scalp electrode single-use	Analytical scalp electrode single-use	Class I
Electroencephalographic monitoring system	Electroencephalographic monitoring system	Class IIa