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 - Ferno Canada

Address:

2460 Tedlo Street

Ontario

l5a3v3

Canada

Authorised Representative/ UK Responsible Person
Name: Ferno (UK) Limited
Address:

Ferno House Stubs Beck Lane West 26 Industrial Estate

Cleckheaton

West Yorkshire BD19 4TZ

United Kingdom

Code/Term Type

Cardiac compression board Cardiac compression board Class I

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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