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 - Ryser Optik AG

Address:

Metzgergasse 2

CH-9004 St. Gallen

CH-9004

Switzerland

Authorised Representative/ UK Responsible Person
Name: HAAG STREIT UK LTD
Address:

Unit A Cartel Business Estate

EDINBURGH WAY

HARLOW

ESSEX CM20 2TT

United Kingdom

Code/Term Type

Spectacle lens foil Spectacle lens foil Class I

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.