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 - Vitrolife Inc. San Diego

Address:

6835 Flanders Drive Suite 500

San Diego

California 92121

United States

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

1 Chapel Street

Warwick

CV34 4HL

England United Kingdom

Code/Term Type

User-induced micropipette User-induced micropipette Class I

Microscope counting chamber IVD Microscope counting chamber IVD 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
User-induced micropipette	User-induced micropipette	Class I
Microscope counting chamber IVD	Microscope counting chamber IVD	IVD General