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 - EYEVAN Inc.

Address:

1-15-33 Minami-aoyama Minaoto-ku

Tokyo

107-0062

Japan

Authorised Representative/ UK Responsible Person
Name: AF PHARMA SERVICE UK LTD
Address:

Suite 140 Temple Chambers 3-7 Temple Avenue

London

EC4Y 0DA

England United Kingdom

Code/Term Type

Spectacle frame Spectacle frame 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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