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 - Novartis Pharma AG

Address:

Lichstrasse 35

Basel

4056

Switzerland

Authorised Representative/ UK Responsible Person
Name: Novartis Pharmaceuticals UK Limited
Address:

2nd Floor The Westworks Building White City Place

195 Wood Lane

London

W12 7FQ

England United Kingdom

Code/Term Type

General-purpose syringe single-use General-purpose syringe single-use Class I

Metered dose inhaler Metered dose inhaler

Intraocular injection kit Intraocular injection kit Class I

Intraocular injection kit Intraocular injection kit

Intraocular injection kit Intraocular injection kit 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
General-purpose syringe single-use	General-purpose syringe single-use	Class I
Metered dose inhaler	Metered dose inhaler
Intraocular injection kit	Intraocular injection kit	Class I
Intraocular injection kit	Intraocular injection kit
Intraocular injection kit	Intraocular injection kit	Class IIa