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 - HOYA Medical Singapore Pte Ltd

Address:

455A Jalan Ahmad Ibrahim

Singapore

639939

Singapore

Authorised Representative/ UK Responsible Person
Name: Hoya Lens UK Ltd
Address:

Industrial Estate Wrexham

Cross Lanes

LL13 9UA.

United Kingdom

Code/Term Type

Intraocular lens calculation software Intraocular lens calculation software Class I

Posterior-chamber intraocular lens pseudophakic Posterior-chamber intraocular lens pseudophakic 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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Code/Term		Type
Intraocular lens calculation software	Intraocular lens calculation software	Class I
Posterior-chamber intraocular lens pseudophakic	Posterior-chamber intraocular lens pseudophakic	Class IIb