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

Back to MHRA

Manufacturer's Devices - Wake Up International B.V.

Address:

Bergweg 49

Zeist

3707 AA

Netherlands

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

Livingstone House 309 Harrow Road

Wembley

Middlesex HA9 6BD

England United Kingdom

Code/Term Type

Hearing aid disinfector Hearing aid disinfector 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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