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 - Implantica CE Reflux Ltd

Address:

Sir Temi Zammit Buildings Malta Life Sciences Park

San Gwann

SGN 3000

Malta

Authorised Representative/ UK Responsible Person
Name: MT Promedt Consulting Ltd
Address:

Beaver House 23-38 Hythe Bridge Street

Oxford

OX1 2EP

England United Kingdom

Code/Term Type

Gastro-oesophageal antireflux fundal implant placement tool reusable Gastro-oesophageal antireflux fundal implant placement tool reusable Class I

Gastro-oesophageal antireflux extraluminal fundal implant Gastro-oesophageal antireflux extraluminal fundal implant Class IIb

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
Gastro-oesophageal antireflux fundal implant placement tool reusable	Gastro-oesophageal antireflux fundal implant placement tool reusable	Class I
Gastro-oesophageal antireflux extraluminal fundal implant	Gastro-oesophageal antireflux extraluminal fundal implant	Class IIb