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 - NordicNeuroLab AS

Address:

Møllendalsveien 1

Bergen

5009

Norway

Authorised Representative/ UK Responsible Person
Name: QAdvis UK Ltd
Address:

55-66 Frederick Street

Edinburgh EH2 1LS

EH2 1LS

Scotland United Kingdom

Code/Term Type

Interactive-evaluation patient hand-controller Interactive-evaluation patient hand-controller Class I

Visual stimulator Visual stimulator Class I

MRI system synchronizer MRI system synchronizer Class I

MRI system application software MRI system application software Class I

MRI system application software MRI system application software Class I

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
Interactive-evaluation patient hand-controller	Interactive-evaluation patient hand-controller	Class I
Visual stimulator	Visual stimulator	Class I
MRI system synchronizer	MRI system synchronizer	Class I
MRI system application software	MRI system application software	Class I
MRI system application software	MRI system application software	Class I