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 - Carl Zeiss Meditec Inc.

Address:

5300 Central Parkway

Dublin

Alameda/CA 94568

United States

Authorised Representative/ UK Responsible Person
Name: Carl Zeiss Ltd
Address:

Zeiss House 1030 Cambourne Business Park

Cambourne

Cambridgeshire CB23 6DW

England United Kingdom

Code/Term Type

Perimeter automatic Perimeter automatic Class IIa

Retinal optical coherence tomography system Retinal optical coherence tomography system Class IIa

Corneal topography system Corneal topography system Class IIa

Ophthalmic spectral-domain optical coherence tomography system Ophthalmic spectral-domain optical coherence tomography system Class IIa

Ophthalmic fundus camera Ophthalmic fundus camera Class IIa

Perimeter automatic Perimeter automatic 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
Perimeter automatic	Perimeter automatic	Class IIa
Retinal optical coherence tomography system	Retinal optical coherence tomography system	Class IIa
Corneal topography system	Corneal topography system	Class IIa
Ophthalmic spectral-domain optical coherence tomography system	Ophthalmic spectral-domain optical coherence tomography system	Class IIa
Ophthalmic fundus camera	Ophthalmic fundus camera	Class IIa
Perimeter automatic	Perimeter automatic	Class I