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 - Diasoft B.V.

Address:

Klepelhoek 11

Leusden

Utrecht 3833 GZ

Netherlands

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Nephrology information system application software Nephrology information system application software Class IIb

Nephrology information system application software Nephrology information system application software Class IIb

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
Nephrology information system application software	Nephrology information system application software	Class IIb
Nephrology information system application software	Nephrology information system application software	Class IIb