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 - Ensemble Medical Manufacturers Pty

Address:

35/36F Kyalami Industrial Park Kyalami Road

Westmead 35/36F Kyalami Industrial Park

Durban

Durban 3605

South Africa

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

4 Limecroft View Wingerworth

Chesterfield

S42 6NR

England United Kingdom

Code/Term Type

Pressure bandage non-latex single-use Pressure bandage non-latex single-use Class I

Cardiopulmonary resuscitation mask single-use Cardiopulmonary resuscitation mask single-use Class I

Cardiopulmonary resuscitation mask single-use Pressure bandage non-latex single-use Conformity Assessment Certificate Expired 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
Pressure bandage non-latex single-use	Pressure bandage non-latex single-use	Class I
Cardiopulmonary resuscitation mask single-use	Cardiopulmonary resuscitation mask single-use	Class I
Cardiopulmonary resuscitation mask single-use	Pressure bandage non-latex single-use Conformity Assessment Certificate Expired	Class I