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

Back to MHRA

Manufacturer's Devices - Eli Lilly and Company_ Pharmaceutical Delivery Systems

Address:

Eli Lilly and Company _Pharmaceutical Delivery Systems Lilly Corporate Center

Indianapolis

Indianapolis

IN 46285

United States

Authorised Representative/ UK Responsible Person
Name: Eli Lilly and Company Ltd
Address:

Lilly House Basing View

Basingstoke

Hampshire RG21 4FA

England United Kingdom

Code/Term Type

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

Patient monitoring system module data memory Patient monitoring system module data memory Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Cartridge-accepting autoinjector mechanical	Cartridge-accepting autoinjector mechanical	Class IIb
Patient monitoring system module data memory	Patient monitoring system module data memory	Class I