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 - Shanxi Regent Works Inc

Address:

No.9 Xinhe Road Private Economic Zone Taiyuan

Shanxi Province

030043

China

Authorised Representative/ UK Responsible Person
Name: SUNGO Certification Company Limited
Address:

3rd Floor 70 Gracechurch Street

London

EC3V 0HR

England United Kingdom

Code/Term Type

Lumbar spine orthosis Lumbar spine orthosis Class I

Tubular support bandage non-latex reusable Tubular support bandage non-latex reusable Class I

Wrist orthosis Wrist orthosis Class I

Elbow orthosis Elbow orthosis Class I

Ankle/foot orthosis Ankle/foot 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
Lumbar spine orthosis	Lumbar spine orthosis	Class I
Tubular support bandage non-latex reusable	Tubular support bandage non-latex reusable	Class I
Wrist orthosis	Wrist orthosis	Class I
Elbow orthosis	Elbow orthosis	Class I
Ankle/foot orthosis	Ankle/foot orthosis	Class I