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 - AMO Uppsala AB

Address:

Rapsgatan 7 Box 6406

Uppsala

SE-75136

Sweden

Authorised Representative/ UK Responsible Person
Name: AMO UNITED KINGDOM LIMITED
Address:

Pinewood Campus Nine Mile Ride

Wokingham

Berkshire RG40 3EW

United Kingdom

Code/Term Type

Vitreous/aqueous humour replacement medium intraoperative Vitreous/aqueous humour replacement medium intraoperative 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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