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 - Omnimate Enterprise Co Ltd

Address:

No 8 Ln. 126 Sec. 2 Ligon 1st Road

Wujie Township

Yilan County 268015

Taiwan

Authorised Representative/ UK Responsible Person
Name: Marshall Airway Products Ltd
Address:

Suite 3H1 St Peters Park Cobblers Way

Westfield

Radstock

BA3 3BX

England United Kingdom

Code/Term Type

Nasopharyngeal airway single-use Nasopharyngeal airway single-use Class IIa

Emergency airway clearance suction system manual Emergency airway clearance suction system manual 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
Nasopharyngeal airway single-use	Nasopharyngeal airway single-use	Class IIa
Emergency airway clearance suction system manual	Emergency airway clearance suction system manual	Class I