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 - Ki Mobility

Address:

5201 Woodward Drive Stevens Point

Wisconsin

54481

United States

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

Etac Limited Unit 60 Hartlebury Trading Estate

Hartlebury

Kidderminster

Kidderminster DY10 4JD

England United Kingdom

Code/Term Type

Wheelchair occupant-driven rear-wheels-operated non-collapsible Wheelchair occupant-driven rear-wheels-operated non-collapsible Class I

Wheelchair back rest Wheelchair back rest Class I

Wheelchair seat cushion Wheelchair seat cushion Class I

Push-rim manual wheelchair non-bariatric Push-rim manual wheelchair non-bariatric 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
Wheelchair occupant-driven rear-wheels-operated non-collapsible	Wheelchair occupant-driven rear-wheels-operated non-collapsible	Class I
Wheelchair back rest	Wheelchair back rest	Class I
Wheelchair seat cushion	Wheelchair seat cushion	Class I
Push-rim manual wheelchair non-bariatric	Push-rim manual wheelchair non-bariatric	Class I