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

Back to MHRA

Manufacturer's Devices - Serrix B.V.

Address:

Herengracht 458 CA

Amsterdam

1017

Netherlands

Authorised Representative/ UK Responsible Person
Name: Profoot (UK) Ltd
Address:

Unit G Penfold Works Imperial Way

Watford

Hertfordshire WD24 4YY

United Kingdom

Code/Term Type

Nail infection solution Nail infection solution Class I

Nail fungus treatment kit non-medicated Nail fungus treatment kit non-medicated Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Nail infection solution	Nail infection solution	Class I
Nail fungus treatment kit non-medicated	Nail fungus treatment kit non-medicated	Class IIa