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 - Shandong Blue Sail Innovation Co. Ltd

Address:

East Side of Xing'an Road Sixth Phase Project Zone Dongcheng Sub-district Offices

Linqu

Shandong 262600

China

Authorised Representative/ UK Responsible Person
Name: lotus global co ltd
Address:

23 Maine Street

Reading

Reading RG2 6AG

England United Kingdom

Code/Term Type

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

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