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 - PMD Device Solutions Ltd t/a PMD Solutions

Address:

Bishopstown House Model Farm Road

Cork

T12 T922

Ireland

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

129 Great Tattenhams Epsom Downs

Epsom

Surrey KY18 5RB

England United Kingdom

Code/Term Type

Patient monitoring system module respiratory Patient monitoring system module respiratory 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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