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 - Keeler USA (Accutome Inc)

Address:

3222 Phoenixville Pike Building 50

Malvern

Pennsylvania 19355

United States

Authorised Representative/ UK Responsible Person
Name: Keeler Ltd
Address:

Clewer Hill Road

Windsor

Berkshire SL4 4AA

United Kingdom

Code/Term Type

Ophthalmic tonometer probe Ophthalmic tonometer probe 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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