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 - PEPE Pty Ltd

Address:

100 Campbell Street

Brisbane

QLD 4006

Australia

Authorised Representative/ UK Responsible Person
Name: GMASIA UK LTD
Address:

65 London Wall

London

EC2M 5TU

England 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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