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 - Menicon B.V.

Address:

Waanderweg 6

Emmen

7812 HZ

Netherlands

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

Soft corrective contact lens daily-wear Soft corrective contact lens daily-wear Class IIa

Rigid-gas-permeable corrective contact lens daily-wear Rigid-gas-permeable corrective contact lens daily-wear 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
Soft corrective contact lens daily-wear	Soft corrective contact lens daily-wear	Class IIa
Rigid-gas-permeable corrective contact lens daily-wear	Rigid-gas-permeable corrective contact lens daily-wear	Class IIa