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 - Fidia Farmaceutici S.p.A.

Address:

Via Ponte della Fabbrica 3/A

Padua

Abano Terme 35031

Italy

Authorised Representative/ UK Responsible Person
Name: Purple Orchid Health limited
Address:

Albany House 14 Shute End

Wokingham

RB40 1BJ

England United Kingdom

Code/Term Type

Vaginal mucosa protection dressing Vaginal mucosa protection dressing Class IIa

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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