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 - Medical iSight Corporation

Address:

7th Floor 767 Third Avenue

New York

10017

United States

Authorised Representative/ UK Responsible Person
Name: Medical iSight (UK) Limited
Address:

9th Floor 107 Cheapside

London

EC2V 6DN

England United Kingdom

Code/Term Type

Surgical planning/navigation-enhancement system Surgical planning/navigation-enhancement 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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