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 - Tiaset di Carresi Lorenzo

Address:

via delle cantine 30

San Cipriano Cavriglia

Arezzo 52022

Italy

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Patient surgical drape single-use Patient surgical drape single-use Class III

Patient surgical drape single-use Patient surgical drape single-use 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
Patient surgical drape single-use	Patient surgical drape single-use	Class III
Patient surgical drape single-use	Patient surgical drape single-use	Class IIa