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 - SPD Swiss Precision Diagnostics GmbH

Address:

47 route de Saint-Georges

Petit-Lancy

1213

Switzerland

Authorised Representative/ UK Responsible Person
Name: SPD Development Company Limited
Address:

Priory Business Park

Bedford

Bedfordshire MK44 3UP

England United Kingdom

Code/Term Type

Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid Class B – Self-testing or Near-patient Testing

Natural conception assistance kit Natural conception assistance kit IVD Devices for Self-Testing

Natural conception assistance kit Natural conception assistance kit IVD Devices for Self-Testing

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
Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid	Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid	Class B – Self-testing or Near-patient Testing
Natural conception assistance kit	Natural conception assistance kit	IVD Devices for Self-Testing
Natural conception assistance kit	Natural conception assistance kit	IVD Devices for Self-Testing