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 - Keiser Corporation

Address:

2470 S. Cherry Ave

Fresno

California 93706

United States

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

Unit 3 Hampton Industrial Estate Hampton Street

Tetbury

Gloucestershire GL8 8LD

England United Kingdom

Code/Term Type

Bicycle exerciser Bicycle exerciser Class I

Upper-limb mechanical weight exerciser lever/pulley-cable Upper-limb mechanical weight exerciser lever/pulley-cable Class I

Chest-press exerciser Chest-press exerciser Class I

Core-body mechanical weight exerciser Core-body mechanical weight exerciser Class I

Back pulldown exerciser Back pulldown exerciser Class I

Lower-limb mechanical weight exerciser Lower-limb mechanical weight exerciser 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
Bicycle exerciser	Bicycle exerciser	Class I
Upper-limb mechanical weight exerciser lever/pulley-cable	Upper-limb mechanical weight exerciser lever/pulley-cable	Class I
Chest-press exerciser	Chest-press exerciser	Class I
Core-body mechanical weight exerciser	Core-body mechanical weight exerciser	Class I
Back pulldown exerciser	Back pulldown exerciser	Class I
Lower-limb mechanical weight exerciser	Lower-limb mechanical weight exerciser	Class I