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 - HertARTAps

Address:

Gustaf Werners gata 2

Västra Frölunda

42132

Sweden

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

1 Chapel Street

Warwick

CV34 4HL

England United Kingdom

Code/Term Type

User-induced pipette User-induced pipette Class IIa

Assisted reproduction procedure dish Assisted reproduction procedure dish Class IIa

Assisted reproduction centrifuge tube Assisted reproduction centrifuge tube 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
User-induced pipette	User-induced pipette	Class IIa
Assisted reproduction procedure dish	Assisted reproduction procedure dish	Class IIa
Assisted reproduction centrifuge tube	Assisted reproduction centrifuge tube	Class IIa