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 - Centervue SpA

Address:

Via San Marco 9H

Padova

35129

Italy

Authorised Representative/ UK Responsible Person
Name: Mainline Instruments LTD
Address:

Unit 2 Cyclo Works Lifford Lane

Kings Norton

Birmingham

West Midlands B30 3DY

United Kingdom

Code/Term Type

Ophthalmic fundus camera Ophthalmic fundus camera Class IIa

Perimeter automatic Perimeter automatic Class I

Perimeter automatic Perimeter automatic 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
Ophthalmic fundus camera	Ophthalmic fundus camera	Class IIa
Perimeter automatic	Perimeter automatic	Class I
Perimeter automatic	Perimeter automatic	Class IIa