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 - Shenzhen Lifotronic Technology Co. Ltd.

Address:

Unit A 4th Floor Building 15 Yijing Estate No.1008 Songbai Road Nanshan District

Shenzhen

518055

China

Authorised Representative/ UK Responsible Person
Name: Umedwings UK LTD
Address:

291 Brighton Road

South Croydon

CR2 6EQ

England United Kingdom

Code/Term Type

Irrigation negative-pressure wound therapy unit Irrigation negative-pressure wound therapy unit Class IIa

Negative-pressure wound therapy system foam dressing non-antimicrobial Negative-pressure wound therapy system foam dressing non-antimicrobial Class IIb

Intermittent venous compression system Intermittent venous compression system Class IIa

Chest-oscillation airway secretion-clearing system Chest-oscillation airway secretion-clearing system 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
Irrigation negative-pressure wound therapy unit	Irrigation negative-pressure wound therapy unit	Class IIa
Negative-pressure wound therapy system foam dressing non-antimicrobial	Negative-pressure wound therapy system foam dressing non-antimicrobial	Class IIb
Intermittent venous compression system	Intermittent venous compression system	Class IIa
Chest-oscillation airway secretion-clearing system	Chest-oscillation airway secretion-clearing system	Class IIa