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 - DMD

Address:

1 Rue de l’Espoir

Lezennes

59260

France

Authorised Representative/ UK Responsible Person
Name: Ecolab Ltd
Address:

PO BOX 11 NORTHWICH CHESHIRE UK PO BOX 11

Winnington Avenue

Northwich

Cheshire CW8 4DX

England United Kingdom

Code/Term Type

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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