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

Back to MHRA

Manufacturer's Devices - Vapotherm Inc.

Address:

100 Domain Drive

Exeter

New Hampshire 03833

United States

Authorised Representative/ UK Responsible Person
Name: AJW Technology Consulting Ltd
Address:

4/4a Bloomsbury Square

London

WC1A 2RP

England United Kingdom

Code/Term Type

Respiratory oxygen therapy pulse oximeter-regulator interface Respiratory oxygen therapy pulse oximeter-regulator interface Class IIb

Professional high-flow respiratory unit humidifying Professional high-flow respiratory unit humidifying Class IIa

Nasal oxygen cannula basic Nasal oxygen cannula basic Class IIa

Negative-pressure face tent Negative-pressure face tent Class IIa

Intravenous pole Intravenous pole Class I

Intravenous pole Intravenous pole 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
Respiratory oxygen therapy pulse oximeter-regulator interface	Respiratory oxygen therapy pulse oximeter-regulator interface	Class IIb
Professional high-flow respiratory unit humidifying	Professional high-flow respiratory unit humidifying	Class IIa
Nasal oxygen cannula basic	Nasal oxygen cannula basic	Class IIa
Negative-pressure face tent	Negative-pressure face tent	Class IIa
Intravenous pole	Intravenous pole	Class I
Intravenous pole	Intravenous pole	Class IIa