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 - Soleko S.p.A

Address:

Via Ravano s.n.c

Pontecorvo (FR)

03037

Italy

Authorised Representative/ UK Responsible Person
Name: Menicon Ltd
Address:

1 Gatelodge Close Round Spinney Industrial Estate

Northampton

Northamptonshire NN3 8RJ

United Kingdom

Code/Term Type

Posterior-chamber intraocular lens pseudophakic Posterior-chamber intraocular lens pseudophakic Class IIb

Contact lens disinfecting solution Contact lens disinfecting solution Class IIb

Multi-purpose soft/rigid contact lens solution Multi-purpose soft/rigid contact lens solution 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
Posterior-chamber intraocular lens pseudophakic	Posterior-chamber intraocular lens pseudophakic	Class IIb
Contact lens disinfecting solution	Contact lens disinfecting solution	Class IIb
Multi-purpose soft/rigid contact lens solution	Multi-purpose soft/rigid contact lens solution	Class IIb