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 - Streifeneder ortho.production GmbH

Address:

Moosfeldstraße 10

Emmering

Bavaria 82275

Germany

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Ankle/foot orthosis Ankle/foot orthosis Class I

External limb prosthesis socket liner External limb prosthesis socket liner Class I

Stump sock Stump sock Class I

External lower-limb prosthesis structural/alignment component External lower-limb prosthesis structural/alignment component Class I

Hydraulic/pneumatic external knee prosthesis Hydraulic/pneumatic external knee prosthesis Class I

Mechanical-resistance external ankle-foot prosthesis Mechanical-resistance external ankle-foot prosthesis 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
External limb prosthesis socket liner	External limb prosthesis socket liner	Class I
Stump sock	Stump sock	Class I
External lower-limb prosthesis structural/alignment component	External lower-limb prosthesis structural/alignment component	Class I
Hydraulic/pneumatic external knee prosthesis	Hydraulic/pneumatic external knee prosthesis	Class I
Mechanical-resistance external ankle-foot prosthesis	Mechanical-resistance external ankle-foot prosthesis	Class I