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 - Vitalitec International Inc. d/b/a Peters Surgical USA

Address:

10 Cordage Park Circle Suite 100/200

Plymouth

MA 02360

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

Intravascular anastomosis occluder Intravascular anastomosis occluder Class IIa

Clamp jaw cover Clamp jaw cover Class IIa

Surgical bulldog clamp single-use Surgical bulldog clamp single-use Class IIa

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 anastomosis occluder	Intravascular anastomosis occluder	Class IIa
Clamp jaw cover	Clamp jaw cover	Class IIa
Surgical bulldog clamp single-use	Surgical bulldog clamp single-use	Class IIa