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 - St Andrews Medical Innovations Limited

Address:

Walter Bower House Eden Campus

Main Street Guardbridge

St Andrews

Fife KY16 0US

Scotland United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Direct ophthalmoscope Direct ophthalmoscope Class I

Indirect binocular ophthalmoscope Indirect binocular ophthalmoscope 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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Code/Term		Type
Direct ophthalmoscope	Direct ophthalmoscope	Class I
Indirect binocular ophthalmoscope	Indirect binocular ophthalmoscope	Class I