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 - Visiometrics S.L.

Address:

Vinyals 131

Terrassa

08221

Spain

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

Clewer Hill Road

Windsor

Berkshire SL4 4AA

United Kingdom

Code/Term Type

Retinoscope line-powered Retinoscope line-powered Class IIa

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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