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 - Teleflex Medical Private Limited

Address:

R.S. No-23 Thirubuvanai Mannadipet Commune

Puducherry

605 107

India

Authorised Representative/ UK Responsible Person
Name: TFX Group Ltd (T/A Teleflex Medical UK)
Address:

Grosvenor House Horseshoe Crescent

Old Town Beaconsfield

Buckinghamshire HP9 1LJ

England United Kingdom

Code/Term Type

Indwelling urethral drainage balloon catheter non-antimicrobial Indwelling urethral drainage balloon catheter non-antimicrobial 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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