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 - Silipos Holding LLC

Address:

7049 Williams Rd.

Niagara Falls

New York NY14304

United States

Authorised Representative/ UK Responsible Person
Name: WMDE Uk Ltd.
Address:

The New Barn Mill Lane Eastry

Sandwich

CT13 0JW

England United Kingdom

Code/Term Type

Pressure-management bandage padded Pressure-management bandage padded 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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