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 - VascoMed GmbH

Address:

Hertzallee 1

Binzen

79589

Germany

Authorised Representative/ UK Responsible Person
Name: BIOTRONIK UK LIMITED
Address:

BIOTRONIK House Avonbury Business Park

Bicester

OX26 2UA

United Kingdom

Code/Term Type

Cardiac radio-frequency ablation system catheter Cardiac radio-frequency ablation system catheter Class III

Cardiac mapping catheter percutaneous single-use Cardiac mapping catheter percutaneous single-use 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 radio-frequency ablation system catheter	Cardiac radio-frequency ablation system catheter	Class III
Cardiac mapping catheter percutaneous single-use	Cardiac mapping catheter percutaneous single-use	Class III