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

Address:

Fannin House South County Business Park

Leopardstown Fannin House

Dublin

D18 Y0C9

Ireland

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

Yeo Bank 3 Kenn road

Clevedon

Somerset BS21 6TH

United Kingdom

Code/Term Type

Nitrile examination/treatment glove non-powdered non-antimicrobial Nitrile examination/treatment glove non-powdered non-antimicrobial Class I

Hevea-latex examination/treatment glove non-powdered non-antimicrobial Hevea-latex examination/treatment glove non-powdered non-antimicrobial Class I

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
Nitrile examination/treatment glove non-powdered non-antimicrobial	Nitrile examination/treatment glove non-powdered non-antimicrobial	Class I
Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Class I