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 - Eschenbach Optik GmbH

Address:

Fürther Str. 252

Nürnberg

90429

Germany

Authorised Representative/ UK Responsible Person
Name: Stuart Baldwin & Susan Pringle Trading as Associated Optical Products
Address:

Gore House 13 Gore Road

Burnham

Burnham

Buckinghamshire SL1 8AA

England United Kingdom

Code/Term Type

Hand-held magnifier Hand-held magnifier Class I

Spectacle frame Spectacle frame 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
Hand-held magnifier	Hand-held magnifier	Class I
Spectacle frame	Spectacle frame	Class I