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 - WaveForm EU d.o.o.

Address:

Obrtna cesta 18

Šentjernej

8310

Slovenia

Authorised Representative/ UK Responsible Person
Name: AgaMatrix Europe Limited
Address:

Harwell Innovation Centre 173 Curie Avenue

Harwell Oxford

DIDCOT

Oxfordshire OX11 0QG

England United Kingdom

Code/Term Type

Percutaneous interstitial-fluid glucose monitoring system electrochemical Percutaneous interstitial-fluid glucose monitoring system electrochemical 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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