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 - Viomedex Limited

Address:

Units 12 - 14 Swan Barn Business Centre

Hailsham

East Sussex BN27 2BY

United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Respiratory apnoea monitoring system Respiratory apnoea monitoring system Class I

Amniotic membrane perforator single-use Amniotic membrane perforator single-use Class I

Skin marking guide single-use Skin marking guide single-use Class I

Ventilator breathing circuit single-use Ventilator breathing circuit single-use Class IIa

Heated respiratory humidifier Heated respiratory humidifier Class IIa

Nasal oxygen cannula CPAP Nasal oxygen cannula CPAP Class IIa

Infant head cap Infant head cap 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
Respiratory apnoea monitoring system	Respiratory apnoea monitoring system	Class I
Amniotic membrane perforator single-use	Amniotic membrane perforator single-use	Class I
Skin marking guide single-use	Skin marking guide single-use	Class I
Ventilator breathing circuit single-use	Ventilator breathing circuit single-use	Class IIa
Heated respiratory humidifier	Heated respiratory humidifier	Class IIa
Nasal oxygen cannula CPAP	Nasal oxygen cannula CPAP	Class IIa
Infant head cap	Infant head cap	Class I