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 - Footmaxx Inc

Address:

518 Pocahontas Ave. NE

Roanoke

Virginia 24012

United States

Authorised Representative/ UK Responsible Person
Name: Eurolink (Europe) Limited
Address:

Milestone House Longcot Road

Shrivenham

Swindon

Wilts SN6 8AL

United Kingdom

Code/Term Type

Orthotic insole custom-made Orthotic insole custom-made Class I

Orthotic shoe custom-made Orthotic shoe custom-made 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
Orthotic insole custom-made	Orthotic insole custom-made	Class I
Orthotic shoe custom-made	Orthotic shoe custom-made	Class I