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 - PhysIOL s.a.

Address:

Liège Science Park Allée des noisetiers 4

Angleur

Liège 4031

Belgium

Authorised Representative/ UK Responsible Person
Name: Beaver-Visitec International Ltd
Address:

Waterloo Industrial Estate

Bidford on Avon

Warwickshire B50 4JH

England United Kingdom

Code/Term Type

Intraocular lens calculation software Intraocular lens calculation software Conformity Assessment Certificate Expired Class I

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

Manual intraocular lens injector single-use Manual intraocular lens injector single-use Class IIa

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.

Code/Term		Type
Intraocular lens calculation software	Intraocular lens calculation software Conformity Assessment Certificate Expired	Class I
Posterior-chamber intraocular lens pseudophakic	Posterior-chamber intraocular lens pseudophakic	Class IIb
Manual intraocular lens injector single-use	Manual intraocular lens injector single-use	Class IIa