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 - Communication and Power Industries Canada

Address:

45 River Drive

Georgetown

Ontario L7G 2J4

Canada

Authorised Representative/ UK Responsible Person
Name: CPI Europe Limited
Address:

Swallowfield Way

Hayes

Middlesex UB3 1DQ

England United Kingdom

Code/Term Type

Diagnostic x-ray system generator mobile Diagnostic x-ray system generator mobile Class IIb

Diagnostic x-ray system generator stationary Diagnostic x-ray system generator stationary Class IIb

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
Diagnostic x-ray system generator mobile	Diagnostic x-ray system generator mobile	Class IIb
Diagnostic x-ray system generator stationary	Diagnostic x-ray system generator stationary	Class IIb