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 - PathRight Medical Inc.

Address:

14252 23rd Ave N.

Plymouth

MN 55447

United States

Authorised Representative/ UK Responsible Person
Name: CASUS UKRP LTD
Address:

107-111 Fleet Street

London

EC4A 2AB

England United Kingdom

Code/Term Type

Penile traction splint Penile traction splint 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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