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 - Givas S.r.l

Address:

Viale Veneto 2 Z.A.

Villatora di Saonara

PD 35020

Italy

Authorised Representative/ UK Responsible Person
Name: Caremed Alrick UK Ltd
Address:

Port Stanley House 5 Falkland Close

Coventry

West Midlands CV4 8AU

England United Kingdom

Code/Term Type

General examination/treatment chair manual General examination/treatment chair manual Class I

General examination/treatment chair electric General examination/treatment chair electric 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
General examination/treatment chair manual	General examination/treatment chair manual	Class I
General examination/treatment chair electric	General examination/treatment chair electric	Class I