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 - Nestmedic S.A.

Address:

Pasymska 20

Warszawa

PL-01-993

Poland

Authorised Representative/ UK Responsible Person
Name: MDSS-UK RP LIMITED
Address:

6 Wilmslow Road Rusholme

Manchester

M14 5TP

England United Kingdom

Code/Term Type

Cardiotocography telemetric monitoring system transmitter Cardiotocography telemetric monitoring system transmitter Class IIa

Obstetrical monitoring/analysis software Obstetrical monitoring/analysis software 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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Code/Term		Type
Cardiotocography telemetric monitoring system transmitter	Cardiotocography telemetric monitoring system transmitter	Class IIa
Obstetrical monitoring/analysis software	Obstetrical monitoring/analysis software	Class IIa