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Post-market review of face masks: Overview
The Therapeutic Goods Administration (TGA) is undertaking a post-market review of face masks included in the Australian Register of Therapeutic Goods (ARTG). This page introduces the review and provides guidance for suppliers and users of face masks. For outcomes of the review, including a list of cancelled ARTG entries, see Post-market review of face masks: Cancelled ARTG entries.
Background to the review
COVID-19 has increased the demand and supply of personal protective equipment (PPE) such as face masks and respirators, gloves, face shields, goggles, and gowns designed to protect the wearer from the spread of disease, illness and infection.
Some of these products meet the definition of a medical device and so must be included in the ARTG before being supplied. Some products do not meet the definition of a medical device and, while they may still be used to prevent the spread of diseases including COVID-19, they do not need to be included in the ARTG.
For more information about the use and regulation of PPE, including face masks and respirators, please review:
- Regulation of Personal Protective Equipment and COVID-19
- Advice on surgical masks and gowns during COVID-19.
Due to a rapid increase in demand for the manufacturing, importation and sale of face masks, there has been an increase in medical device inclusions in the ARTG, with many manufactured and imported from overseas.
Concerns have been raised about the quality and effectiveness of some products, particularly face masks, including that they:
- are included in the ARTG but do not meet the legislative requirements for medical devices; or
- may not, or do not, perform as intended.
The TGA post-market review of face masks will validate if the devices included in the ARTG through the auto-inclusion process meet all the regulatory requirements and perform as intended.
On 22 March 2020, the Therapeutic Goods (Medical Devices—Face Masks and Other Articles) (COVID-19 Emergency) Exemption 2020 was made to support the purchase of certain kinds of medical devices by the Australian Government Department of Health for the National Medical Stockpile. The emergency exemption continues to support the Australian Government's rapid COVID-19 response by facilitating access to certain kinds of medical devices intended to assist in reducing the transmission of infection between individuals, particularly patients and health care professionals.
The masks in the National Medical Stockpile will be included in our post-market review.
The TGA is aware of recently identified issues with some filtering face piece respirators that claim compliance as KN95 respirators against the Chinese national standard for Respiratory Protection, GB 2626.
There are concerns these devices may not provide consistent and adequate respiratory protection based on testing conducted by National Institute for Occupational Safety and Health (NIOSH) - National Personal Protective Technology Laboratory (NPPTL) of the Centers for Disease Control and Prevention (CDC).
If you supply face masks
If you are the legal entity responsible for importing and supplying face masks (ie: the sponsor), you must ensure all regulatory requirements relating to your products are met. You should also:
- Determine if your product meets the definition of a medical device. If your product does meet the definition of a medical device, you should ensure it is included in the ARTG before you import and/or supply it.
- Ensure you have the following evidence available to provide to the TGA when requested as part of the post-market review:
- declaration of conformity (conformity assessment certificate)
- a list of models of masks, supply numbers by model and year (if applicable), and the states within Australia where you have distributed the face masks
- details of the manufacturing standards the devices conform to and evidence of compliance
- a copy of all packaging and labelling
- a copy of the Instructions for Use that are supplied with your product (if applicable)
- where the intended purpose of the device claims to protect the wearer from COVID-19, either specifically or by implication, appropriate evidence to support such a claim (for example, evidence from a clinical trial, or testing from an accredited laboratory to a recognised standard).
If you are the supplier of a medical device in Australia, it is your responsibility to ensure all regulatory requirements are met.
There are civil and criminal penalties associated with supplying a medical device that is not included in the ARTG or subject to an exemption, and for providing false or misleading information to the TGA.
If you are supplying a device that does not meet the regulatory requirements, the TGA strongly recommends that you contact the TGA, or cease supply and cancel your ARTG inclusion.
If you use face masks
Only personal protective equipment (PPE) for therapeutic use are required to be in the ARTG. For example, surgical or examination masks intended to reduce or prevent the transmission of disease or micro-organisms (such as bacteria or viruses) are medical devices. These products are regulated by the TGA and are required to be included in the ARTG before they can be supplied.
If you are a consumer of these products, you should familiarise yourself with the differences in available face masks and be aware of the manner in which these products are used in order to maximise the protection they can offer. In particular:
- While other languages can also be used, medical devices must be supplied with the labels, packaging and Instructions for Use in English.
- The name and address of the supplier, and the name of the manufacturer, should be provided on the packaging or label.
- You can check if a face mask is included in the ARTG by searching the ARTG using the name of the person or company legally responsible for the product (ie: the sponsor). Product names are not available in the ARTG.
- Face masks are supplied as both medical devices and as personal protection for use in industrial settings. Ratings such as N95 and P2 relate to standards that may not be associated with a therapeutic use. You should familiarise yourself with the specific claims and ratings associated with the product you are using to ensure it is appropriate for the manner in which you intend to use it. Standards Australia has published a Summary of information on standards and conformance for PPE products that outlines the factors assessed under each standard.
- Ensure you always use your medical device in the manner intended by the manufacturer by following the Instructions for Use.
- Be aware of potentially counterfeit devices. Look at product markings, such as the name of the manufacturer, to determine whether anything is amiss (incorrect spelling, faded packaging, incorrect filters/materials, etc.).
The TGA has online forms for reporting any concerns or issues:
- Report a perceived breach or questionable practices, including the sale of unauthorised products.
- Report potentially false or misleading advertising.
- Report a problem with a medical device.
For frequently asked questions and more information about reporting medical device adverse events, see Medical device incident reporting & investigation scheme (IRIS).