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 - Eyerising International Pty Ltd

Address:

Suite 2.05 9-11 Claremont Street

South Yarra Victoria

3141

Australia

Authorised Representative/ UK Responsible Person
Name: MedEther Limited
Address:

Kemp House 160 City Road

London

EC1V 2NX

England United Kingdom

Code/Term Type

Home-use myopia control red light device Home-use myopia control red light device 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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