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 - IB Medical AB

Address:

Rundelgatan 2

Tranas

573 35

Sweden

Authorised Representative/ UK Responsible Person
Name: TR Equipment UK Ltd
Address:

c/o EBS Ltd. Innovation Centre

Gallows Hill

Warwick

Warwickshire CV34 6UW

England United Kingdom

Code/Term Type

Lumbosacral spine orthosis hernia support Lumbosacral spine orthosis hernia support Class I

Haemorrhoidal cryotherapy device single-use Haemorrhoidal cryotherapy device single-use Class I

Haemorrhoidal cryotherapy device reusable Haemorrhoidal cryotherapy device reusable Class I

Localized cutaneous/musculoskeletal cryotherapy unit Localized cutaneous/musculoskeletal cryotherapy unit Class I

Oral mucositis cryotherapy mouthpiece Oral mucositis cryotherapy mouthpiece 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
Lumbosacral spine orthosis hernia support	Lumbosacral spine orthosis hernia support	Class I
Haemorrhoidal cryotherapy device single-use	Haemorrhoidal cryotherapy device single-use	Class I
Haemorrhoidal cryotherapy device reusable	Haemorrhoidal cryotherapy device reusable	Class I
Localized cutaneous/musculoskeletal cryotherapy unit	Localized cutaneous/musculoskeletal cryotherapy unit	Class I
Oral mucositis cryotherapy mouthpiece	Oral mucositis cryotherapy mouthpiece	Class I