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 - Quirem Medical B.V.

Address:

Zutphenseweg 55

Deventer

7418 AH

Netherlands

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

Otium House 2 Freemantle Road

Bagshot

Surrey GU19 5LL

England United Kingdom

Code/Term Type

Radiology DICOM image processing application software Radiology DICOM image processing application software Class IIb

Manual brachytherapy source permanent implant Manual brachytherapy source permanent implant

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
Radiology DICOM image processing application software	Radiology DICOM image processing application software	Class IIb
Manual brachytherapy source permanent implant	Manual brachytherapy source permanent implant