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 - The Focal Rooms by The Bilbro & Co Co.

Address:

125-127 Manchester Road

GBR

SOUTHPORT

Merseyside PR9 9BD

United Kingdom

Authorised Representative/ UK Responsible Person
Name:
Address:

Code/Term Type

Prescribed Spectacles and contact lens kits

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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