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 - DIERS International GmbH

Address:

Dillenbergweg 4

Schlangenbad

65388

Germany

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Footrest Footrest Class I

Body-surface pressure mapping system Body-surface pressure mapping system Class I

Electromyography monitor Electromyography monitor Class I

Myograph Myograph Class I

Standard treadmill powered Standard treadmill powered Class I

Radiological video camera patient positioning/tracking system Radiological video camera patient positioning/tracking system Class I

Biomechanical function analysis system motion-tracking Biomechanical function analysis system motion-tracking 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
Footrest	Footrest	Class I
Body-surface pressure mapping system	Body-surface pressure mapping system	Class I
Electromyography monitor	Electromyography monitor	Class I
Myograph	Myograph	Class I
Standard treadmill powered	Standard treadmill powered	Class I
Radiological video camera patient positioning/tracking system	Radiological video camera patient positioning/tracking system	Class I
Biomechanical function analysis system motion-tracking	Biomechanical function analysis system motion-tracking	Class I