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 - MediPurpose Pte.Ltd.

Address:

10 Anson Road #12-08 International Plaza

Singapore

079903

Singapore

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Manual scalpel blade single-use Manual scalpel blade single-use Class IIa

Manual blood lancing device single-use Manual blood lancing device single-use Class IIa

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
Manual scalpel blade single-use	Manual scalpel blade single-use	Class IIa
Manual blood lancing device single-use	Manual blood lancing device single-use	Class IIa