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 - Schelchen GmbH

Address:

Im Gewerberpark 4-6

Im Gewerberpark 4-6

Konig Wusterhausen

Berlin - Brandenburg D-15711

Germany

Authorised Representative/ UK Responsible Person
Name: EUROLEATHERS 2000 Ltd
Address:

Ibex House Ferro Fields Brixworth Northampton

Brixworth Industrial Estate Brixworth Northampton

NORTHAMPTON

Northamptonshire NN6 9UA

England United Kingdom

Code/Term Type

Orthotic insole prefabricated non-antimicrobial Orthotic insole prefabricated non-antimicrobial Class I

Heel stirrup cushion/pad Heel stirrup cushion/pad 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 prefabricated non-antimicrobial	Orthotic insole prefabricated non-antimicrobial	Class I
Heel stirrup cushion/pad	Heel stirrup cushion/pad	Class I