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 - Meda Pharma S.p.A

Address:

Meda Pharma S.p.A. Via Valosa di Sopra

Monza

20900

Italy

Authorised Representative/ UK Responsible Person
Name: MYLAN UK HEALTHCARE LIMITED
Address:

20 Station Close

Potters Bar

EN6 1TL

England United Kingdom

Code/Term Type

Wart-removal material Wart-removal material 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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