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 - MEDCAPTAIN MEDICAL TECHNOLOGY CO. LTD.

Address:

12th Floor Baiwang Research Building No.5158 Shahe West Road Xili Nanshan

Shenzhen

Guangdong 518055

China

Authorised Representative/ UK Responsible Person
Name: Etheria Medical Ltd
Address:

The Old brush Factory Unit 2D Whickham Industrial Estate Swalwell

Newcastle Upon Tyne

NE16 3DA

United Kingdom

Code/Term Type

Bedside syringe pump Bedside syringe pump Class IIb

Infusion pump management unit mobile Infusion pump management unit mobile Class IIb

Enteral feeding pump Enteral feeding pump Class IIa

Bedside infusion pump single-channel Bedside infusion pump single-channel Class IIb

Flexible video laryngoscope Flexible video laryngoscope 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
Bedside syringe pump	Bedside syringe pump	Class IIb
Infusion pump management unit mobile	Infusion pump management unit mobile	Class IIb
Enteral feeding pump	Enteral feeding pump	Class IIa
Bedside infusion pump single-channel	Bedside infusion pump single-channel	Class IIb
Flexible video laryngoscope	Flexible video laryngoscope	Class I