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 - Shijiazhuang AOFEITE IMP & EXP Co. Ltd

Address:

No. 202 Plant 4th Layer In Gree Supporting Industrial Park No. 389 Hengshan Street High-tech District Shijiazhuang City

Hebei Province

050000

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

Hip orthosis Hip orthosis Class I

Knee support orthosis Knee support orthosis Class I

Ankle/foot orthosis Ankle/foot orthosis Class I

Lumbar spine orthosis Lumbar spine orthosis Class I

Cervical spine collar reusable Cervical spine collar reusable Class I

Elbow orthosis Elbow orthosis Class I

Wrist orthosis Wrist 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
Hip orthosis	Hip orthosis	Class I
Knee support orthosis	Knee support orthosis	Class I
Ankle/foot orthosis	Ankle/foot orthosis	Class I
Lumbar spine orthosis	Lumbar spine orthosis	Class I
Cervical spine collar reusable	Cervical spine collar reusable	Class I
Elbow orthosis	Elbow orthosis	Class I
Wrist orthosis	Wrist orthosis	Class I