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 - Venclose Inc

Address:

2570 N. First Street 2nd Floor #221

San Jose

CA 95131

United States

Authorised Representative/ UK Responsible Person
Name: ICON (LR) Limited
Address:

Concept House 6 Stoneycroft Rise

Chandlers Ford Eastleigh

Hampshire

SO53 3LD

England United Kingdom

Code/Term Type

Foot-switch electrical Foot-switch electrical Class I

Electrical mains power cable Electrical mains power cable Class I

Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator Conformity Assessment Certificate Expired Class IIb

Peripheral vascular electrocautery catheter single-use Peripheral vascular electrocautery catheter single-use Conformity Assessment Certificate Expired Class IIb

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
Foot-switch electrical	Foot-switch electrical	Class I
Electrical mains power cable	Electrical mains power cable	Class I
Percutaneous radio-frequency ablation system generator	Percutaneous radio-frequency ablation system generator Conformity Assessment Certificate Expired	Class IIb
Peripheral vascular electrocautery catheter single-use	Peripheral vascular electrocautery catheter single-use Conformity Assessment Certificate Expired	Class IIb