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 - Camp Scandinavia AB

Address:

Karbingatan 38

Helsingborg

25467

Sweden

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Ankle/foot orthosis Ankle/foot orthosis Class I

Lumbar spine orthosis Lumbar spine orthosis Class I

Orthosis suspension unit Orthosis suspension unit Class I

Compression/pressure shirt/pants Compression/pressure shirt/pants Class I

Wrist/hand orthosis Wrist/hand orthosis Class I

Knee support orthosis Knee support orthosis Class I

Knee support orthosis Knee support orthosis 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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Code/Term		Type
Ankle/foot orthosis	Ankle/foot orthosis	Class I
Lumbar spine orthosis	Lumbar spine orthosis	Class I
Orthosis suspension unit	Orthosis suspension unit	Class I
Compression/pressure shirt/pants	Compression/pressure shirt/pants	Class I
Wrist/hand orthosis	Wrist/hand orthosis	Class I
Knee support orthosis	Knee support orthosis	Class I
Knee support orthosis	Knee support orthosis	Class I