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 - Ontecklong (Nanjing) Medical Supply Corporation Limited

Address:

Building 5 No. 2 Future Road

Park Zhongshan

Nanjing

Jiangsu Liuhe District

China

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

15 Station Road Cross Hills

Keighley

West Yorkshire BD20 7DT

England United Kingdom

Code/Term Type

Eye pad Eye pad 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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