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 - KOO MEDICAL EQUIPMENT(Shanghai) Co. Ltd

Address:

100 Zhongde Road Xiaokunshan Town Songjiang

Shanghai

201614

China

Authorised Representative/ UK Responsible Person
Name: MedPath Limited
Address:

27 Old Gloucester Street

London

WC1N 3AX

England United Kingdom

Code/Term Type

Anaesthesia face mask single-use Anaesthesia face mask single-use Class IIa

CPAP/BPAP face mask single-use CPAP/BPAP face mask single-use Class IIa

Anaesthesia breathing circuit single-use Anaesthesia breathing circuit single-use 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
Anaesthesia face mask single-use	Anaesthesia face mask single-use	Class IIa
CPAP/BPAP face mask single-use	CPAP/BPAP face mask single-use	Class IIa
Anaesthesia breathing circuit single-use	Anaesthesia breathing circuit single-use	Class IIa