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 - PreAnalytiX

Address:

Garstligweg 8 Hombrechtikon

Hombrechtikon

Meilen 8634

Switzerland

Authorised Representative/ UK Responsible Person
Name: QIAGEN Manchester Ltd.
Address:

QIAGEN Manchester Ltd. Citylabs 2.0

200 Hathersage Road

Manchester

M13 0BH

England United Kingdom

Code/Term Type

Evacuated blood collection tube IVD nucleic acid stabilizer Evacuated blood collection tube IVD nucleic acid stabilizer IVD General

Nucleic acid extraction/isolation kit IVD Nucleic acid extraction/isolation kit IVD IVD General

Nucleic acid extraction/isolation kit IVD Nucleic acid extraction/isolation kit IVD Class A

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
Evacuated blood collection tube IVD nucleic acid stabilizer	Evacuated blood collection tube IVD nucleic acid stabilizer	IVD General
Nucleic acid extraction/isolation kit IVD	Nucleic acid extraction/isolation kit IVD	IVD General
Nucleic acid extraction/isolation kit IVD	Nucleic acid extraction/isolation kit IVD	Class A