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 - Royal Fornia Medical Equipment Co. Ltd.

Address:

Fornia Tech Park NO.18 Kejiyi Road Hi-Tech innovation Coast Tangjia Bay

Zhuhai

Guangdong 519085

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

Endobronchial tube Endobronchial tube Class IIa

Laryngeal mask airway single-use Laryngeal mask airway single-use Class IIa

Laryngeal mask airway single-use Laryngeal mask airway 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
Endobronchial tube	Endobronchial tube	Class IIa
Laryngeal mask airway single-use	Laryngeal mask airway single-use	Class IIa
Laryngeal mask airway single-use	Laryngeal mask airway single-use	Class IIa