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 Medical Device Co. Ltd.

Address:

East and southwest side in the fourth floor in the NO.202 of Gree supporting industrial park No.389 of Hengshan street High-tech Zone

Hebei

Shijiazhuang 050000

China

Authorised Representative/ UK Responsible Person
Name: FN INTERNATIONAL LIMITED
Address:

Wisteria Grange Barn Pikes End

Pinner

Middlesex HA5 2EX

England United Kingdom

Code/Term Type

Lumbosacral spine orthosis hernia support Lumbosacral spine orthosis hernia support 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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