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 - Harvard Medical Devices Ltd

Address:

Units 1002 10th Floor Railway Plaza

39 Chatham Road South Tsimshatsui

Hong Kong

Kowloon 999007

China

Authorised Representative/ UK Responsible Person
Name: Kinetik Medical Devices Ltd
Address:

Lockeridge house lockeridge

malborough

malborough

Wiltshire sn84el

England United Kingdom

Code/Term Type

Patient monitoring system module blood pressure noninvasive Patient monitoring system module blood pressure noninvasive Class IIa

Infrared patient thermometer ear/skin Infrared patient thermometer ear/skin Class IIa

Red-light phototherapy unit battery-powered Red-light phototherapy unit battery-powered Class IIa

Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation 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
Patient monitoring system module blood pressure noninvasive	Patient monitoring system module blood pressure noninvasive	Class IIa
Infrared patient thermometer ear/skin	Infrared patient thermometer ear/skin	Class IIa
Red-light phototherapy unit battery-powered	Red-light phototherapy unit battery-powered	Class IIa
Analgesic transcutaneous electrical nerve stimulation system	Analgesic transcutaneous electrical nerve stimulation system	Class IIa