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 - F Care Systems NV

Address:

Uitbreidingstraat 42-46

Berchem

Antwerp B-2600

Belgium

Authorised Representative/ UK Responsible Person
Name: Qarad UK Ltd.
Address:

8 Northumberland Ave

Westminster

London WC2N 5BY

England United Kingdom

Code/Term Type

Endoscopic electrosurgical electrode monopolar single-use Endoscopic electrosurgical electrode monopolar single-use Class IIb

Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator Class IIb

Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator 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
Endoscopic electrosurgical electrode monopolar single-use	Endoscopic electrosurgical electrode monopolar single-use	Class IIb
Percutaneous radio-frequency ablation system generator	Percutaneous radio-frequency ablation system generator	Class IIb
Percutaneous radio-frequency ablation system generator	Percutaneous radio-frequency ablation system generator	Class IIa