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 - SW Sustainability Solutions Inc.

Address:

33278 Central Ave Ste 102

Union City

California 94587

United States

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Hevea-latex examination/treatment glove non-powdered non-antimicrobial Hevea-latex examination/treatment glove non-powdered non-antimicrobial Class I

Polychloroprene examination/treatment glove non-powdered Polychloroprene examination/treatment glove non-powdered Class I

Nitrile examination/treatment glove non-powdered non-antimicrobial Nitrile examination/treatment glove non-powdered non-antimicrobial 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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Code/Term		Type
Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Class I
Polychloroprene examination/treatment glove non-powdered	Polychloroprene examination/treatment glove non-powdered	Class I
Nitrile examination/treatment glove non-powdered non-antimicrobial	Nitrile examination/treatment glove non-powdered non-antimicrobial	Class I