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 - Sodel

Address:

190 rue Rene Barthelemy

Lisieux

14100

France

Authorised Representative/ UK Responsible Person
Name: Alkapharm UK Limited
Address:

266-268 Stratford Road Shirley

Solihull

Solihull

B90 3AD

England United Kingdom

Code/Term Type

Medical device disinfection agent Medical device disinfection agent Class IIb

Medical device cleaning/disinfection wipe Medical device cleaning/disinfection wipe Class IIb

Medical device cleaning agent Medical device cleaning agent 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
Medical device disinfection agent	Medical device disinfection agent	Class IIb
Medical device cleaning/disinfection wipe	Medical device cleaning/disinfection wipe	Class IIb
Medical device cleaning agent	Medical device cleaning agent	Class I