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 - Fizimed SAS

Address:

8 Rue Sainte Marguerite

STRASBOURG

67000

France

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

Southfields Road

Dunstable

Beds LU6 3EJ

England United Kingdom

Code/Term Type

Pelvic floor exercise biofeedback device Pelvic floor exercise biofeedback device Class I

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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