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 - MedOne Surgical Inc.

Address:

670 Tallevast Road

Sarasota

FL 34243

United States

Authorised Representative/ UK Responsible Person
Name: Eye Technology Ltd
Address:

19 Totman Crescent Brook Road Industrial Estate

Rayleigh

Essex SS6 7UY

United Kingdom

Code/Term Type

Ophthalmic irrigation/infusion/aspiration cannula non-illuminating single-use Ophthalmic irrigation/infusion/aspiration cannula non-illuminating single-use Class IIa

Ophthalmic knife single-use Ophthalmic knife single-use Class IIa

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
Ophthalmic irrigation/infusion/aspiration cannula non-illuminating single-use	Ophthalmic irrigation/infusion/aspiration cannula non-illuminating single-use	Class IIa
Ophthalmic knife single-use	Ophthalmic knife single-use	Class IIa