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 - DARCO (Europe) GmbH

Address:

Gewerbegebiet 18

Raisting

82399

Germany

Authorised Representative/ UK Responsible Person
Name: V-M Orthotics Ltd
Address:

Unit 25 Halesworth Business Centre

Norwich Road

Halesworth

Suffolk IP19 8QJ

England United Kingdom

Code/Term Type

Ankle/foot orthosis Ankle/foot orthosis Class I

Foot cushion Foot cushion Class I

Toe separator Toe separator Class I

Orthotic shoe non-customized Orthotic shoe non-customized Class I

Orthotic insole prefabricated non-antimicrobial Orthotic insole prefabricated non-antimicrobial 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
Ankle/foot orthosis	Ankle/foot orthosis	Class I
Foot cushion	Foot cushion	Class I
Toe separator	Toe separator	Class I
Orthotic shoe non-customized	Orthotic shoe non-customized	Class I
Orthotic insole prefabricated non-antimicrobial	Orthotic insole prefabricated non-antimicrobial	Class I