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 - AMK Medical Equipment Co Ltd

Address:

3rd Floor B14 Huachuang Industry Area

Jinshin Cun Shiji Town

Guangzhou

Panyu District n/a

China

Authorised Representative/ UK Responsible Person
Name: Marshall Airway Products Ltd
Address:

Suite 3H1 St Peters Park Cobblers Way

Westfield

Radstock

BA3 3BX

England United Kingdom

Code/Term Type

Basic endotracheal tube single-use Basic endotracheal tube single-use Class IIa

Reinforced endotracheal tube single-use Reinforced endotracheal tube single-use Class IIa

Cuff-suction endotracheal tube Cuff-suction endotracheal tube Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Basic endotracheal tube single-use	Basic endotracheal tube single-use	Class IIa
Reinforced endotracheal tube single-use	Reinforced endotracheal tube single-use	Class IIa
Cuff-suction endotracheal tube	Cuff-suction endotracheal tube	Class IIa