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 - Yangzhou Medline Industry Co. Ltd.

Address:

No. 108 Jinshan Road Economic Development Zone

Yangzhou Jiangsu

225009

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

General-purpose syringe single-use General-purpose syringe single-use Class IIa

Metered-delivery hypodermic syringe/needle Metered-delivery hypodermic syringe/needle Class IIa

Subcutaneous infusion/injection port needle Subcutaneous infusion/injection port needle Class IIa

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
General-purpose syringe single-use	General-purpose syringe single-use	Class IIa
Metered-delivery hypodermic syringe/needle	Metered-delivery hypodermic syringe/needle	Class IIa
Subcutaneous infusion/injection port needle	Subcutaneous infusion/injection port needle	Class IIa