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 - RIMSA P. LONGONI SRL

Address:

Via Monte Rosa 18-20-22 Seregno

MB

Lombardia 20831

Italy

Authorised Representative/ UK Responsible Person
Name: MDQ Services Ltd
Address:

Flat 81 Seacon Tower 5 Hutching’s Street

London

England E14 8JX

England United Kingdom

Code/Term Type

Operating room light Operating room light Class I

Operating room light system Operating room light system 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
Operating room light	Operating room light	Class I
Operating room light system	Operating room light system	Class I