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 - Rayner Intraocular Lenses Limited

Address:

The Ridley Innovation Centre 10 dominion Way

Worthing West Sussex

West Sussex

BN14 8AQ

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

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

Vitreous/aqueous humour replacement medium intraoperative Vitreous/aqueous humour replacement medium intraoperative Class IIb

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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Code/Term		Type
Posterior-chamber intraocular lens pseudophakic	Posterior-chamber intraocular lens pseudophakic	Class IIb
Vitreous/aqueous humour replacement medium intraoperative	Vitreous/aqueous humour replacement medium intraoperative	Class IIb
Vitreous/aqueous humour replacement medium intraoperative	Vitreous/aqueous humour replacement medium intraoperative	Class IIb