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 - Turon Medtech AB

Address:

Kardanvägen 21

Varberg

SE-43232

Sweden

Authorised Representative/ UK Responsible Person
Name: Siemens Healthcare Limited
Address:

Park View Watchmoor Park

Camberley

Hampshire GU15 3YL

England United Kingdom

Code/Term Type

Needle guide single-use Needle guide single-use Class I

Needle guide single-use Needle guide single-use Class I

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
Needle guide single-use	Needle guide single-use	Class I
Needle guide single-use	Needle guide single-use	Class I