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 - UNEEG medical A/S

Address:

Borupvang 2

Allerød

3450

Denmark

Authorised Representative/ UK Responsible Person
Name: UNEEG medical UK Ltd
Address:

12 New Fetter Lane

London

EC4A 1JP

England United Kingdom

Code/Term Type

Electroencephalography telemetric monitoring system Electroencephalography telemetric monitoring system

Electroencephalography telemetric monitoring system Electroencephalography telemetric monitoring system Class I

Electroencephalography telemetric monitoring system Electroencephalography telemetric monitoring system Class I

Electroencephalography telemetric monitoring system Electroencephalography telemetric monitoring system

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
Electroencephalography telemetric monitoring system	Electroencephalography telemetric monitoring system
Electroencephalography telemetric monitoring system	Electroencephalography telemetric monitoring system	Class I
Electroencephalography telemetric monitoring system	Electroencephalography telemetric monitoring system	Class I
Electroencephalography telemetric monitoring system	Electroencephalography telemetric monitoring system