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 - H. + H. Maslanka Chirurgische Instrumente GmbH

Address:

Stockacher Straße 172

Tuttlingen

78532

Germany

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 occluder/interatrial shunt transcatheter introducer Cardiac occluder/interatrial shunt transcatheter introducer 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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