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 - Diacor Inc

Address:

1236 South Airstrip Lane

Diacor Inc

Mount Pleasant

UT 84647

United States

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

Summit House 4-5 Mitchell Street

Edinburgh

EH6 7BD

Scotland United Kingdom

Code/Term Type

Patient transfer system powered Patient transfer system powered 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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