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 - Fannin Ltd (LIP)

Address:

Fannin Ltd (LIP) IDA Industrial Estate

Ballybrit Upper

Galway

Galway H91 FD9E

Ireland

Authorised Representative/ UK Responsible Person
Name: Fannin (UK) Ltd
Address:

Unit 100 Westminster Industrial Estate

Repton Road Measham

Swadlincote

Derbyshire DE12 7DT

United Kingdom

Code/Term Type

Enriched agar culture medium IVD Enriched agar culture medium IVD IVD General

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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