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:

Feldbachstrasse Hombrechtikon

Hombrechtikon

Meilen 8634

Switzerland

Serilization:

Authorised Representative
Name: QIAGEN Manchester Ltd
Address:

Skelton House Lloyd Street North

Manchester

Greater Manchester M15 6SH

United Kingdom

Code/Term Type

Evacuated blood collection tube IVD, nucleic acid stabilizer 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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