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 - mySugr GmbH

Address:

Trattnerhof 1/5 OG

Vienna

1010

Austria

Authorised Representative/ UK Responsible Person
Name: Roche Diabetes Care Ltd.
Address:

Charles Avenue Burgess Hill RH15 9RY

Burgess Hill

RH15 9RY

United Kingdom

Code/Term Type

Self-care monitoring/reporting software Self-care monitoring/reporting software Class IIa

Ambulatory insulin infusion pump software patient-dosing Ambulatory insulin infusion pump software patient-dosing Class IIb

Ambulatory insulin infusion pump software patient-dosing Ambulatory insulin infusion pump software patient-dosing 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
Self-care monitoring/reporting software	Self-care monitoring/reporting software	Class IIa
Ambulatory insulin infusion pump software patient-dosing	Ambulatory insulin infusion pump software patient-dosing	Class IIb
Ambulatory insulin infusion pump software patient-dosing	Ambulatory insulin infusion pump software patient-dosing	Class IIb