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 - Compression Works Inc

Address:

Compression Works Inc 1634-A Montgomery Hwy

#115

Birmingham

35216

United States

Authorised Representative/ UK Responsible Person
Name: Callisto Regulatory Consulting Limited
Address:

The Barn Holly Berry House Rough Park

Rugeley

Staffordshire WS15 3SQ

England United Kingdom

Code/Term Type

Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set 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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