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 - Occlutech Tibbi Urunler San.ve Tic.Ltd.Sti

Address:

Yeilköy SB Mah. E Blok Sok. Occlutech Apt. No:6

Bakrköy/stanbul

34149

Turkey

Authorised Representative/ UK Responsible Person
Name: Occlutech UK Ltd
Address:

Lynton House 7-12 Tavistock Square

London

London

WC1H9LT

United Kingdom

Code/Term Type

Cardiac defect occluder Cardiac defect occluder Class III

Cardiac occluder delivery kit Cardiac occluder delivery kit Class III

Interatrial shunt Interatrial shunt Class III

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
Cardiac defect occluder	Cardiac defect occluder	Class III
Cardiac occluder delivery kit	Cardiac occluder delivery kit	Class III
Interatrial shunt	Interatrial shunt	Class III