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 - SparMED ApS

Address:

Ryttermarken 2

Farum

3520

Denmark

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

The Old School

Tresillian

Tresillian

Cornwall TR2 4BA

England United Kingdom

Code/Term Type

Medical device disinfection agent Medical device disinfection agent Class IIa

Medical device cleaning/disinfection wipe Medical device cleaning/disinfection wipe Class IIa

Medical gas pipeline system air filter Medical gas pipeline system air filter Class I

General specimen container IVD no additive/medium General specimen container IVD no additive/medium IVD General

Centrifuge tube IVD sterile Centrifuge tube IVD sterile IVD General

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
Medical device disinfection agent	Medical device disinfection agent	Class IIa
Medical device cleaning/disinfection wipe	Medical device cleaning/disinfection wipe	Class IIa
Medical gas pipeline system air filter	Medical gas pipeline system air filter	Class I
General specimen container IVD no additive/medium	General specimen container IVD no additive/medium	IVD General
Centrifuge tube IVD sterile	Centrifuge tube IVD sterile	IVD General