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 - V. Guldmann A/S

Address:

Graham Bells Vej 21-23A

Aarhus N.

8200

Denmark

Authorised Representative/ UK Responsible Person
Name: European Device Solutions Ltd
Address:

15 COANWOOD DRIVE Whitley Bay

WHITLEY BAY

TYNE AND WEAR NE25 9GB

England United Kingdom

Code/Term Type

Overhead track patient lifting/transfer system Overhead track patient lifting/transfer system Class I

Mobile patient lifting system manual Mobile patient lifting system manual Class I

Manual patient lifting belt/harness Manual patient lifting belt/harness Class I

Patient lifting system stretcher Patient lifting system stretcher Class I

Portable ramp Portable ramp 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
Overhead track patient lifting/transfer system	Overhead track patient lifting/transfer system	Class I
Mobile patient lifting system manual	Mobile patient lifting system manual	Class I
Manual patient lifting belt/harness	Manual patient lifting belt/harness	Class I
Patient lifting system stretcher	Patient lifting system stretcher	Class I
Portable ramp	Portable ramp	Class I