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

Back to MHRA

Manufacturer's Devices - ZRT Laboratory

Address:

8605 SW Creekside Place

Beaverton

OR 97008

United States

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

Sandford Gate East Point Business Park

Oxford

OX4 6LB

England United Kingdom

Code/Term Type

General specimen container IVD no additive/medium General specimen container IVD no additive/medium IVD General

Non-evacuated urine specimen container IVD no additive Non-evacuated urine specimen container IVD no additive IVD General

Dried blood spot collection kit IVD Dried blood spot collection kit IVD IVD General

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
General specimen container IVD no additive/medium	General specimen container IVD no additive/medium	IVD General
Non-evacuated urine specimen container IVD no additive	Non-evacuated urine specimen container IVD no additive	IVD General
Dried blood spot collection kit IVD	Dried blood spot collection kit IVD	IVD General