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 - Otech Industry SRL

Address:

Corso Felice Cavallotti 60

1521 Alessandria

1521

Italy

Authorised Representative/ UK Responsible Person
Name: Hospital Innovations Limited
Address:

Concept House 1 Heol Y Twyn Talbot Green Business Park

Talbot Green

Rhondda Cynon Taff CF72 9FG

Wales United Kingdom

Code/Term Type

Electrosurgical/ultrasonic surgical system generator Electrosurgical/ultrasonic surgical system generator Class IIb

Electrosurgical handpiece reusable Electrosurgical handpiece reusable Class IIb

Electrosurgical return lead Electrosurgical return lead Class IIb

Foot-switch electrical Foot-switch electrical 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
Electrosurgical/ultrasonic surgical system generator	Electrosurgical/ultrasonic surgical system generator	Class IIb
Electrosurgical handpiece reusable	Electrosurgical handpiece reusable	Class IIb
Electrosurgical return lead	Electrosurgical return lead	Class IIb
Foot-switch electrical	Foot-switch electrical	Class IIb