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 - HumanOptics Holding AG

Address:

Spardorfer Str. 150

Erlangen

91054

Germany

Authorised Representative/ UK Responsible Person
Name: Kestrel Ophthalmics Ltd
Address:

Unit 9 Cabot Business Village Holyrood Close

Poole

Dorset BH17 7BA

United Kingdom

Code/Term Type

Posterior-chamber intraocular lens pseudophakic Posterior-chamber intraocular lens pseudophakic Class IIb

Contact details

Freedom of information

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

© 2011 Crown Copyright. To contact us about this website, use our feedback form.