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 - Monidor Oy

Address:

Elektroniikkatie 3

Oulu

90590

Finland

Authorised Representative/ UK Responsible Person
Name: PENTLAND MEDICAL LTD
Address:

157 Broomhall Crescent

EDINBURGH

EH12 7PJ

Scotland United Kingdom

Code/Term Type

Intravenous gravity infusion monitor Intravenous gravity infusion monitor 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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