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 - AcuFocus Inc.

Address:

32 Discovery Suite 200

Irvine

CA92618

United States

Authorised Representative/ UK Responsible Person
Name: Medpace UK Ltd.
Address:

Vintners Place 68 Upper Thames St Queenhithe

London

EC4V 3BJ

England United Kingdom

Code/Term Type

Posterior-chamber intraocular lens pseudophakic extended-focus Posterior-chamber intraocular lens pseudophakic extended-focus Class IIb

Posterior-chamber intraocular lens pseudophakic extended-focus Posterior-chamber intraocular lens pseudophakic extended-focus

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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Code/Term		Type
Posterior-chamber intraocular lens pseudophakic extended-focus	Posterior-chamber intraocular lens pseudophakic extended-focus	Class IIb
Posterior-chamber intraocular lens pseudophakic extended-focus	Posterior-chamber intraocular lens pseudophakic extended-focus