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 - Access Point Technologies EP Inc.

Address:

12560 Fletcher Lane #300

Rogers

Minnesota 55374

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Electrical-only medical device connection cable reusable Electrical-only medical device connection cable reusable Class I

Cardiac mapping catheter percutaneous single-use Cardiac mapping catheter percutaneous single-use Class III

Cardiac radio-frequency ablation system catheter Cardiac radio-frequency ablation system catheter 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
Electrical-only medical device connection cable reusable	Electrical-only medical device connection cable reusable	Class I
Cardiac mapping catheter percutaneous single-use	Cardiac mapping catheter percutaneous single-use	Class III
Cardiac radio-frequency ablation system catheter	Cardiac radio-frequency ablation system catheter	Class III