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 - Albrecht GmbH

Address:

Chiemseestrasse 81

Bernau am Chiemsee

83233

Germany

Authorised Representative/ UK Responsible Person
Name: MedEnvoy UK Limited
Address:

85 Great Portland Street First Floor

London

W1W 7LT

England United Kingdom

Code/Term Type

Ankle/foot orthosis Ankle/foot orthosis Class I

Wrist/hand orthosis Wrist/hand orthosis Class I

Elbow joint orthosis component Elbow joint orthosis component Class I

Foot orthosis Foot orthosis Class I

Lumbar spine orthosis Lumbar spine orthosis Class I

Knee support orthosis Knee support orthosis Class I

Thoracic spine orthosis Thoracic spine orthosis Class I

Elbow orthosis Elbow orthosis 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
Wrist/hand orthosis	Wrist/hand orthosis	Class I
Elbow joint orthosis component	Elbow joint orthosis component	Class I
Foot orthosis	Foot orthosis	Class I
Lumbar spine orthosis	Lumbar spine orthosis	Class I
Knee support orthosis	Knee support orthosis	Class I
Thoracic spine orthosis	Thoracic spine orthosis	Class I
Elbow orthosis	Elbow orthosis	Class I