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

Back to MHRA

Manufacturer's Devices - MY01 Inc

Address:

400 Boul De Maisonneuve Ouest Suite 700

Montréal

Quebec H3A 1L4

Canada

Authorised Representative/ UK Responsible Person
Name: UKCApartner4U Limited
Address:

7 CAMPION WAY

BINGHAM NOTTINGHAM

NG13 8 TR

England United Kingdom

Code/Term Type

Compartmental-pressure monitoring system single-use Compartmental-pressure monitoring system single-use Class IIa

Compartmental-pressure monitoring system application software Compartmental-pressure monitoring system application software 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
Compartmental-pressure monitoring system single-use	Compartmental-pressure monitoring system single-use	Class IIa
Compartmental-pressure monitoring system application software	Compartmental-pressure monitoring system application software	Class I