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 - SLK VERTRIEBSGESELLSCHAFT mbH

Address:

Am Herdicksbach 18

Waltrop

D-45731

Germany

Authorised Representative/ UK Responsible Person
Name: Wellell UK Limited
Address:

Unit 33 Great Western Business Park

McKenzie Way Worcester

Worcester

Worcestershire WR4 9GN

England United Kingdom

Code/Term Type

Mobile patient lifting system electrically-powered Mobile patient lifting system electrically-powered Class I

Stand-up mobile patient lifting system electrically-powered Stand-up mobile patient lifting system electrically-powered Class I

Patient lifting system hammock sling Patient lifting system hammock sling Class I

Patient lifting system divided leg sling Patient lifting system divided leg sling 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
Mobile patient lifting system electrically-powered	Mobile patient lifting system electrically-powered	Class I
Stand-up mobile patient lifting system electrically-powered	Stand-up mobile patient lifting system electrically-powered	Class I
Patient lifting system hammock sling	Patient lifting system hammock sling	Class I
Patient lifting system divided leg sling	Patient lifting system divided leg sling	Class I