Compliance & Regulations

Compliance & Regulations

It isn’t as simple as manufacturing and then marketing a medical device in the EU as there are plenty of compliance regulations.

There is a multitude of requirements and which ones apply, depend on the intended use of the device, function, manufacture and others.

There are also a multitude of organisations that have an interest in the public’s health and
safety including the NHS, CCGs, PHE, DHSC, CQC, HSE, FSA and many others.


The LifeVac  ACD is a CLASS I medical device as described in Part II of the UK MDR 2002, Annex IX (as modified by Part II of Schedule 2A to the UK MDR 2002).


EU MDDs or Medical Device Directives are/were designed to harmonise the laws across the EU in relation to medical devices. LifeVac remains compliant with EU MDD and the accompanying EU Directives and Regulations.

UK MDRs or Medical
Device Regulations are specific to the UK and draw from the EU MDD. With the UK leaving the EU changes to the UK MDR are planned. LifeVac remains compliant with the UK MDR and the accompanying UK Directives and Regulations.

CE & UKCA Marking

In order to comply with relevant legislation in the UK, medical devices are required to be CE marked and display the CE logo.

At LifeVac, we didn’t want to “reinvent the wheel” and charge people for different sized devices for different age groups, which is why we source our fully CE accredited masks from very trusted suppliers who already supply thousands of hospitals and healthcare departments around the world. But the LifeVac device is also is fully CE marked/accredited meeting all CE requirements. This means customers have the peace of mind that every part of LifeVac is CE accredited and you only have to purchase one device to treat all age groups in a choking emergency.

At LifeVac we sell thousands of LifeVac devices a day and every LifeVac device goes through a rigorous quality inspection process, adhering to GMP.

Since 1 January 2021, there have been some changes introduced on how medical devices are placed on the market. One of these is the planned replacement of the CE mark with the UK’s own UKCA marking, LifeVac is already UKCA marked/registered.

CE marking will
continue to be recognised in Great Britain until July 2023.


The official guidance
for Medical Devices are known as MEDical DEVice documents.

This guidance covers a wide range of topics including;

Clinical assessment, rationale and evaluation, Safety and Post Market surveillance, Requirements of conformity to relevant standards and legislation.

MEDDEVs are used by manufacturers, Notified Bodies, Competent Authorities and regulators such as the MHRA to ensure the safe and regulated introduction of medical devices.

Not all MEDDEVs are applicable to a device or device type. It is between the manufacturer and the regulator to agree which MEDDEVs are applicable prior to deployment of any device into a market.

LifeVac has worked with the MHRA to agree on which MEDDEVs were applicable.

Once these had been completed, they were subsequently agreed with the regulator.

Some of the principle
considerations have been outlined here, with a particular focus on those that are queried most often.