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 - Rodenstock GmbH

Address:

Elsenheimer Str. 33

Munich

80687

Germany

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

Radius House Anchor Boulavard

Dartford Crossways Business Park

Dartford

Kent DA2 6QH

England United Kingdom

Code/Term Type

Prescription spectacle lens non-customized Prescription spectacle lens non-customized Class I

Pre-prescription spectacle lens Pre-prescription spectacle lens Class I

Colour discrimination prescription spectacle lens Colour discrimination prescription spectacle lens Class I

Tinted spectacle lens prescription standard Tinted spectacle lens prescription standard Class I

Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens 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
Prescription spectacle lens non-customized	Prescription spectacle lens non-customized	Class I
Pre-prescription spectacle lens	Pre-prescription spectacle lens	Class I
Colour discrimination prescription spectacle lens	Colour discrimination prescription spectacle lens	Class I
Tinted spectacle lens prescription standard	Tinted spectacle lens prescription standard	Class I
Tinted non-prescription spectacle lens	Tinted non-prescription spectacle lens	Class I