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 - ReIngenuity Inc

Address:

167 Sands Street Apt 541

Brooklyn

New York 11201

United States

Authorised Representative/ UK Responsible Person
Name: Eurolink (Europe) Limited
Address:

Milestone House Longcot Road

Shrivenham

Swindon

Wilts SN6 8AL

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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