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 - Novo Nordisk Limited

Address:

3 City Place Beehive Ring Road

Gatwick

RH6 0PA

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Subcutaneous self-injection aid Subcutaneous self-injection aid Class I

Needle guard Needle guard Class I

Cartridge-accepting autoinjector mechanical Cartridge-accepting autoinjector mechanical Class IIb

Basic intravenous administration set noninvasive Basic intravenous administration set noninvasive Class IIa

Autoinjector needle Autoinjector needle

Autoinjector needle Autoinjector needle Class IIa

Autoinjector needle Autoinjector needle 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
Subcutaneous self-injection aid	Subcutaneous self-injection aid	Class I
Needle guard	Needle guard	Class I
Cartridge-accepting autoinjector mechanical	Cartridge-accepting autoinjector mechanical	Class IIb
Basic intravenous administration set noninvasive	Basic intravenous administration set noninvasive	Class IIa
Autoinjector needle	Autoinjector needle
Autoinjector needle	Autoinjector needle	Class IIa
Autoinjector needle	Autoinjector needle	Class IIa