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 - Kreatech Biotechnology B.V.

Address:

Vlierweg 20

Amsterdam

1032LG

Netherlands

Authorised Representative/ UK Responsible Person
Name: Leica Microsystems (UK) Limited
Address:

Larch House Woodlands Business Park

Milton Keynes

MK14 6FG

England United Kingdom

Code/Term Type

Nucleic acid hybridization detection IVD kit Nucleic acid hybridization detection IVD kit IVD General

Nucleic acid hybridization detection IVD probe Nucleic acid hybridization detection IVD probe Class A

Nucleic acid hybridization detection IVD probe Nucleic acid hybridization detection IVD probe 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
Nucleic acid hybridization detection IVD kit	Nucleic acid hybridization detection IVD kit	IVD General
Nucleic acid hybridization detection IVD probe	Nucleic acid hybridization detection IVD probe	Class A
Nucleic acid hybridization detection IVD probe	Nucleic acid hybridization detection IVD probe	IVD General