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 - Ventinova Medical B.V

Address:

Ventinova Medical B.V

Meerenakkerplein Eindhoven

Eindhoven

Brabant 5652

Netherlands

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

Silk Point Queens Avenue

Macclesfield

Cheshire SK10 2BB

England United Kingdom

Code/Term Type

Neonatal/adult intensive-care ventilator Neonatal/adult intensive-care ventilator Class IIa

Manual jet ventilation device Manual jet ventilation device Class IIa

Oxygen administration transtracheal catheter Oxygen administration transtracheal catheter Class IIa

Basic endotracheal tube single-use Basic endotracheal tube 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
Neonatal/adult intensive-care ventilator	Neonatal/adult intensive-care ventilator	Class IIa
Manual jet ventilation device	Manual jet ventilation device	Class IIa
Oxygen administration transtracheal catheter	Oxygen administration transtracheal catheter	Class IIa
Basic endotracheal tube single-use	Basic endotracheal tube single-use	Class IIa