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 - WEM Equipamentos Eletrônicos Ltda.

Address:

Rua Marechal Mascarenhas 550 Riberião Preto

São Paulo

14095-120,

Brazil

Authorised Representative/ UK Responsible Person
Name: Medtronic Limited
Address:

Building 9 Croxley Park

Watford

Herts WD18 8WW

England United Kingdom

Code/Term Type

Argon-enhanced electrosurgical system gas delivery unit Argon-enhanced electrosurgical system gas delivery unit Class IIb

Foot-switch electrical Foot-switch electrical Class I

High-pressure medical gas hose High-pressure medical gas hose Class I

Electrosurgical cable adaptor Electrosurgical cable adaptor Class I

Electrical-only medical device connection cable reusable Electrical-only medical device connection cable reusable 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
Argon-enhanced electrosurgical system gas delivery unit	Argon-enhanced electrosurgical system gas delivery unit	Class IIb
Foot-switch electrical	Foot-switch electrical	Class I
High-pressure medical gas hose	High-pressure medical gas hose	Class I
Electrosurgical cable adaptor	Electrosurgical cable adaptor	Class I
Electrical-only medical device connection cable reusable	Electrical-only medical device connection cable reusable	Class I