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 - Reintraocular Inc

Address:

1018 Meridian Avenue Apt 1

Miami Beach

Miami-Dade

FL 33139

United States

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

Unit 2 Witney Way Boldon Business Park

Boldon Colliery

Tyne And Wear NE35 9PE

England United Kingdom

Code/Term Type

Intraocular pressure-reducing system Intraocular pressure-reducing 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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