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 - U.S Pacific Nonwovens Industry Ltd

Address:

181 Wai Yip Street 11/B Yin Da Commercial Building

Kwun Tong

Kowloon

Hong Kong

China

Authorised Representative/ UK Responsible Person
Name: Mangar International Limited
Address:

Unit 2 Presteigne Industrial Estate

Presteigne

Powys LD8 2UF

United Kingdom

Code/Term Type

General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness 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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