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 - AirPhysio Pty Ltd

Address:

43 Greenway Drive Unit 1

Tweed Heads South

NSW 2486

Australia

Authorised Representative/ UK Responsible Person
Name: Luft for Life Ltd
Address:

63 Barley Gate

Leven

HU17 5NT

United Kingdom

Code/Term Type

Positive pressure airway secretion-clearing device Positive pressure airway secretion-clearing device 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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