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 - AB Germa

Address:

Industrigatan 54 - 56

Kristianstad

SE-291 36

Sweden

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

Vacuum-mould patient positioning system Vacuum-mould patient positioning system Class I

Patient transfer sliding mat Patient transfer sliding mat 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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Code/Term		Type
Vacuum-mould patient positioning system	Vacuum-mould patient positioning system	Class I
Patient transfer sliding mat	Patient transfer sliding mat	Class I