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 - SentreHEART

Address:

300 Saginaw Drive

Redwood City

California CA 94063

United States

Authorised Representative/ UK Responsible Person
Name: AtriCure UK limited
Address:

1 Princeton Mews 167-169 London Road

Kingston Upon Thames

Surrey KT2 6PT

England United Kingdom

Code/Term Type

Intravascular occluding balloon catheter image-guided Intravascular occluding balloon catheter image-guided Class III

Open-surgery ligature loop Open-surgery ligature loop Class III

Cardiac/peripheral vascular guidewire single-use Cardiac/peripheral vascular guidewire single-use Class III

Suture cutter single-use Suture cutter single-use Class IIa

Open-surgery ligator guide sheath Open-surgery ligator guide sheath Class IIa

Suture/ligature tightener single-use Suture/ligature tightener single-use Class I

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
Intravascular occluding balloon catheter image-guided	Intravascular occluding balloon catheter image-guided	Class III
Open-surgery ligature loop	Open-surgery ligature loop	Class III
Cardiac/peripheral vascular guidewire single-use	Cardiac/peripheral vascular guidewire single-use	Class III
Suture cutter single-use	Suture cutter single-use	Class IIa
Open-surgery ligator guide sheath	Open-surgery ligator guide sheath	Class IIa
Suture/ligature tightener single-use	Suture/ligature tightener single-use	Class I