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 - AUS systems Pty Ltd

Address:

3

Charles St Allenby Gardens

South Australia

SA 5009

Australia

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

Unit 5b Fisher Industrial Estate Wiggenhall Road

Watford

Hertfordshire WD18 0FN

England United Kingdom

Code/Term Type

Rectal dilator reusable Rectal dilator reusable 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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