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 - Bioxal SA

Address:

Route des Varennes

Chalon sur Saône

71100

France

Authorised Representative/ UK Responsible Person
Name: Schülke & Mayr UK Ltd
Address:

Cygnet House

Sheffield

S9 1AT

England United Kingdom

Code/Term Type

Medical device disinfection agent Medical device disinfection agent Class IIa

Medical device disinfection agent Medical device disinfection agent Class IIb

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 IIa
Medical device disinfection agent	Medical device disinfection agent	Class IIb