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 - Overland Int'l Corporation

Address:

10F No. 91 Ln.136 Sec. 3 Zhongshan Rd. Zhonghe Dist.

New Taipei City

23546

Taiwan

Authorised Representative/ UK Responsible Person
Name: UK APLAN CORPORATION LTD
Address:

Wandle House Associates 47 Wandle House

Wandle Road

CROYDON Surrey

CR0 1DF

England United Kingdom

Code/Term Type

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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