Manufacturer: Product: ID:

A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

applied by manufacturer procedures applied by for non- applicability
Only if the manufacturer applied manufacturer This column to contain direct reference to
Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

1. GENERAL PRINCIPLES
1. Use of medical devices not to compromise health and safety
A medical device is to be designed and produced in a way that ensures that:
(a) the device will not compromise the clinical condition or safety of a patient, or
the safety and health of the user of any other person, when the device is
used on a patient under the conditions and for the purposes for which the
device was intended and, if applicable, by a user with appropriate technical
knowledge, experience, education or training; and
(b) any risks associated with the use of the device are:
(i) acceptable risks when weighed against the intended benefit to the
patient; and
(ii) compatible with a high level of protection of health and safety.
2. Design and construction of medical devices to conform with safety
principles
(1) The solutions adopted by the manufacturer for the design and construction
of a medical device must conform with safety principles, having regard to
the generally acknowledged state of the art.
(2) Without limiting subclause (1), in selecting appropriate solutions for the
design and construction of a medical device so as to minimise any risks
associated with the use of the device, the manufacturer must:
(a) first, identify hazards and associated risks arising from the use of the
device for its intended purpose, and foreseeable misuse of the device;
and
(b) second, eliminate, or reduce, these risks as far as possible by adopting
a policy of inherently safe design and construction; and
(c) third, if appropriate, ensure that adequate protection measures are
taken, including alarms if necessary, in relation to any risks that cannot
be eliminated; and
(d) fourth, inform users of any residual risks that may arise due to any
shortcomings of the protection measures adopted.

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A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

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Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
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* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

3. Medical devices to be suitable for intended purpose
A medical device must:
(a) perform in the way intended by the manufacturer; and
(b) be designed, produced and packaged in a way that ensures that it is
suitable for one or more of the purposes mentioned in the definition of
medical device in subsection 41BD(1) of the Act.
4. Long-term safety
A medical device must be designed and produced in a way that ensures that if:
(a) the device is used within the period, indicated by the manufacturer, in which
the device can be safely used; and
(b) the device is not subjected to stresses that are outside the stresses that can
occur during normal conditions of use; and
(c) the device is regularly maintained and calibrated in accordance with the
manufacturer’s instructions;
the characteristics and performances mentioned in clauses 1, 2 and 3 are not
adversely affected.
5. Medical devices not to be adversely affected by transport or storage
A medical device must be designed, produced and packed in a way that ensures
that the characteristics and performance of the device when it is being used for
its intended purpose will not be adversely affected during transport and storage
that is carried out taking account of the instructions and information provided by
the manufacturer.
6. Benefits of medical devices to outweigh any side effects
The benefits to be gained from the use of a medical device for the performance
intended by the manufacturer must outweigh any undesirable side effects arising
from its use.

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A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

applied by manufacturer procedures applied by for non- applicability
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Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

2. PRINCIPLES ABOUT DESIGN AND CONSTRUCTION

7. Chemical, physical and biological properties
7.1 Choice of materials
In ensuring that the requirements of Part 1 are met in relation to a medical
device, particular attention must be given to:
(a) the chemical and physical properties of the materials used in the device;
and
(b) the compatibility between the materials used and biological tissues, cells
and body fluids;
having regard to the intended purpose of the device.
7.2 Minimisation of risks associated with contaminants and residues
(1) A medical device must be designed, produced and packed in a way that
ensures that any risks associated with contaminants and residues that may
affect a person who is involved in transporting, storing or using the device,
or a patient, are minimised, having regard to the intended purpose of the
device.
(2) In minimising risks, particular consideration must be given to the likely
duration and frequency of any tissue exposure associated with the
transportation, storage or use of the device.
7.3 Ability to be used safely with materials, etc
(1) A medical device must be designed and produced in a way that ensures
that the device can be used safely with any material, substance or gas with
which the device may come into contact during normal use or use in routine
procedures.
(2) If the device is intended to be used to administer medicine, it must be
designed and produced in a way that ensures that the device:
(a) is compatible with the provisions and restrictions applying to the
medicine to be administered; and
(b) allows the medicine to perform as intended.

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A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

applied by manufacturer procedures applied by for non- applicability
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Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

7.4 Verification of incorporated substance
(1) If a medical device incorporates, or is intended to incorporate, as an integral
part, a substance that, if used separately, might be considered to be a
medicine that is intended to act on a patient in a way that is ancillary to the
device:
the safety and quality of the substance must be verified in
accordance with the requirements for medicines; and
(a) the ancillary action of the substance must be verified having regard to
the intended purpose of the device.
(2) For the purposes of this clause, any stable derivative of human blood or
human plasma is considered to be a medicine.
7.5 Minimisation of risks associated with leaching substances
A medical device must be designed and produced in a way that ensures that any
risks associated with substances that may leach from the device are minimised.
7.6 Minimisation of risks associated with ingress or egress of substances
A medical device must be designed and produced in a way that ensures that any
risks associated with unintentional ingress of substances into, or unintentional
egress of substances out of, the device are minimised, having regard to the
nature of the environment in which the device is intended to be used.
8. Infection and microbial contamination
8.1 Minimisation of risk of infection and contamination
(1) A medical device must be designed and produced in a way that ensures
that the risk of infection to a patient, a user, or any other person, is
eliminated or minimised.
(2) The device must be designed in a way that:
(a) allows it to be easily handled; and
(b) if appropriate, minimises contamination of the device by the patient, or
contamination of the patient by the device, during use.

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applied by manufacturer procedures applied by for non- applicability
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Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

8.2 Control of animal, microbial or recombinant tissues, cells and other
substances
(1) This clause applies in relation to a medical device that contains:
(a) tissues, cells or substances m oral origin
an
i that have been rendered
non-viable; and
(b) tissues, cells or substancesrobial
of micor recombinant origin.
(2) If the tissues, cells or substances originated from animals, the animals must
have been subjected to appropriate veterinary controls and supervision,
having regard to the intended use of the tissues, cells or substances.
(3) If the medical device contains tissues, cells or substances of animal origin, a
record must be kept of the country of origin of each animal from which the
tissues, cells or substances originated.
(4) The processing, preservation, testing and handling of tissues, cells or
substances of animal, microbial or recombinant origin must be carried out in
a way that ensures the highest standards of safety for a patient, the user of
the device, and any other person.
(5) In particular, the production process must implement validated methods of
elimination, or inactivation, in relation to viruses and other transmissible
agents.
8.3 Medical devices to be supplied in a sterile state
(1) This clause applies in relation to a medical device that is intended by the
manufacturer to be supplied in a sterile state.
(2) The device must be designed, produced and packed in a way that ensures
that the device is sterile when it is supplied, and will remain sterile, if stored
and transported in accordance with the directions of the manufacturer, until
the protective packaging is opened or damaged.
(3) The device must be produced and sterilised using an appropriate validated
method.
(4) The device must be produced in appropriately controlled conditions.

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A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

applied by manufacturer procedures applied by for non- applicability
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Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

8.4 Medical devices to be supplied in a non-sterile state
(1) A medical device that is intended by the manufacturer to be supplied in a
non-sterile state must be packed in a way that ensures that the device
maintains the level of cleanliness stipulated by the manufacturer.
(2) If the device is intended to be sterilised before it is used, the device must be
packed in a way that:
(a) ensures that the risk of microbial contamination is minimised; and
(b) is suitable, having regard to the method of sterilisation that the manufacturer
indicates is to be used for the device.
8.5 Distinction between medical devices supplied in sterile and non-sterile
state
If a medical device is supplied in both a sterile state and a non-sterile state, the
information provided with the device must clearly indicate whether the device is
in a sterile state or a non-sterile state.
9. Construction and environmental properties
9.1 Medical devices intended to be used in combination with other devices or
equipment
A medical device that is intended by the manufacturer to be used in combination
with another medical device or other equipment (including a connection system)
must be designed and produced in a way that ensures that:
(a) the medical device, and any other device or equipment with which it is used,
operate in a safe way; and
(b) the intended performance of the device, and any other device or equipment
with which it is used, is not impaired.

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applied by manufacturer procedures applied by for non- applicability
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Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

9.2 Minimisation of risks associated with use of medical devices
A medical device must be designed and produced in a way that ensures that, as
far as practicable, the following risks are removed or minimised:
(a) the risk of injury arising from the physical features of the device;
(b) any risks associated with reasonably foreseeable environmental conditions;
(c) the risk of reciprocal interference involving other devices that are normally
used in an investigation or treatment of the kind for which the device is
intended to be used;
(d) any risks arising if maintenance or calibration of the device is not possible;
(e) any risks associated with the ageing of materials used in the device;
(f) any risks associated with the loss of accuracy of any measuring or control
mechanism of the device;
(g) the risk of fire or explosion occurring during normal use of the device, and in
the event of a single fault condition, especially if the device is intended to be
exposed to flammable substances or substances that can cause
combustion.
10. Medical devices with a measuring function
(1) A medical device that has a measuring function must be designed and
produced in a way that ensures that the device provides accurate, precise
and stable measurements within the limits indicated by the manufacturer
and having regard to the intended purpose of the device.
(2) The measurement, monitoring and display scale of the device must be
designed and produced in accordance with ergonomic principles, having
regard to the intended purpose of the device.
(3) The measurements made by the device must be expressed:
(a) in Australian legal units of measurement; or
(b) if the device measures a physical quantity for which no Australian legal unit
of measurement has been prescribed under the National Measurement Act
1960, in units approved by the Secretary for the particular device.
11. Protection against radiation

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Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

11.1 Minimisation of exposure to radiation
A medical device must be designed and produced in a way that ensures that the
exposure of a patient, the user, or any other person, to radiation is minimised,
having regard to the levels of radiation required to enable the device to perform
its therapeutic and diagnostic functions and the intended purpose of the device.
11.2 Medical devices intended to emit radiation
(1) This clause applies in relation to a medical device that is intended by a
manufacturer to emit hazardous levels of visible or invisible radiation
because the emission is necessary for a specific medical purpose, the
benefit of which is considered to outweigh the risks inherent in the emission.
(2) The device must be designed and produced in a way that ensures that the
user can control the level of the emission.
(3) The device must be designed and produced in a way that ensures the
reproducibility and tolerance of relevant variable parameters.
(4) If practicable, the device must be fitted with a visual indicator or an audible
warning, or both, that operates if potentially hazardous levels of radiation
are emitted.
11.3 Minimisation of exposure to unintended radiation
A medical device must be designed and produced in a way that ensures that the
exposure of a patient, the user, or any other person, to the emission of
unintended, stray or scattered radiation is minimised.
11.4 Operating instructions
The operating instructions for a medical device that emits radiation must include
detailed information about the following matters:
(a) the nature of the radiation emitted;
(b) the means by which patients and users can be protected from the radiation;
(c) ways to avoid misusing the device;
(d) ways to eliminate any risks inherent in the installation of the device.

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applied by manufacturer procedures applied by for non- applicability
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Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

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11.5 Medical devices intended to emit ionising radiation – additional
requirements
(1) This clause applies, in addition to clauses 11.1 to 11.4, in relation to a
medical device that is intended by the manufacturer to emit ionising
radiation.
(2) The device must be designed and produced in a way that ensures that, if
practicable, the quantity, geometry and energy distribution (or quality) of
radiation emitted can be controlled and varied, having regard to the
intended purpose of the device.
(3) If the device is intended to be used for diagnostic radiology, the device must
be designed and produced in a way that ensures that, when used in relation
to a patient for a purpose intended by the manufacturer;
(a) the device achieves an appropriate image or output quality for that
purpose; and
(b) the exposure of the patient, or the user, to radiation is minimised.
(4) if the device is intended to be used for therapeutic radiology, the device
must be designed and produced in a way that ensures that the delivered
dose of radiation, the type and energy of the radiation beam, and, if
appropriate, the energy distribution of the radiation beam, can be reliably
controlled and monitored.
12. Medical devices connected to or equipped with an energy source
12.1 Medical devices incorporating electronic programmable systems
A medical device that incorporates an electronic programmable system must be
designed and produced in a way that ensures that:
(a) the performance, reliability, and repeatability of the system are appropriate
for the intended purpose of the device; and
(b) any consequent risks associated with a single fault condition in the system
are minimised.
12.2 Safety dependent on internal power supply
(1) This clause applies in relation to a medical device if the safety of a patient
on whom the device is to be used will depend on an internal power supply
for the device.
(2) The device must be fitted with a means of determining the state of the
power supply.

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Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

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12.3 Safety dependent on external power supply
(1) This clause applies in relation to a medical device if the safety of a patient
on whom the device is to be used will depend on an external power supply
for the device.
(2) The device must be fitted with an alarm system that indicates whether a
power failure has occurred.
12.4 Medical devices intended to monitor clinical parameters
A medical device that is intended by the manufacturer to be used to monitor one
or more clinical parameters of a patient must be fitted with an appropriate alarm
system to warn the user if a situation has developed that could lead to the death
of the patient or a severe deterioration in the state of the patient’s health.
12.5 Minimisation of risk of electromagnetic fields
A medical device must be designed and produced in a way that ensures that the
risk of an electromagnetic field being created that could impair the operation of
other devices or equipment being used in the vicinity of the medical device is
minimised.
12.6 Protection against electrical risks
A medical device must be designed and produced in a way that ensures that, as
far as possible, when the device is installed correctly, and the device is being
used for an intended purpose under normal conditions of use and in the event of
a single fault condition, patients, users, and any other persons, are protected
against the risk of accidental electric shock.
12.7 Protection against mechanical risks
A medical device must be designed and produced in a way that ensures that a
patient, the users and any other person, is protected against any mechanical
risks associated with the use of the device.
12.8 Protection against risks associated with vibration
(1) A medical device must be designed and produced in a way that ensures
that any risks associated with vibrations generated by the device are
minimised.
(2) If vibrations are not part of the intended performance of the device,
particular attention must be given to relevant technical progress, and the
available means, for limiting vibrations, particularly at source.

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applied by manufacturer procedures applied by for non- applicability
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Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

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12.9 Protection against risks associated with noise
(1) A medical device must be designed and produced in a way that ensures
that any risks associated with noise emitted by the device are minimised.
(2) If noise is not part of the intended performance of the device, particular
attention must be given to relevant technical progress, and the available
means, for reducing the emission of noise, particularly at source.
12.10 Protection against risks associated with terminals and connectors
A medical device that is intended by the manufacturer to be connected to an
electric, gas, hydraulic, pneumatic or other energy supply must be designed and
produced in a way that ensures that any risks to the user associated with the
handling of a terminal or connector on the device, in relation to the energy supply
are minimised.
12.11 Protection against risks associated with heat
A medical device must be designed and produced in a way that ensures that,
during normal use, any accessible part of the device (other than any part
intended by the manufacturer to supply heat or reach a given temperature), and
any area surrounding an accessible part of the device, does not reach a
potentially dangerous temperature.

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Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
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12.12 Protection against risks associated with administration of energy or
substances
(1) This clause applies in relation to a medical device that is intended by the
manufacturer to be used to administer energy or a substance to a patient.
(2) The device must be designed and produced in a way that ensures that:
(a) the delivered rate and amount of energy or of the substance can be set
and maintained accurately to ensure the safety of the patient and the
user; and
(b) as far as possible, the accidental release of dangerous levels of energy
or of the substance is prevented.
(3) the device must be fitted with a means of indicating or, if appropriate,
preventing inadequacies in the rate and amount of energy or of the
substance administered that might cause danger to the patient, the user or
any other person.
(4) The functions of each control and indicator on the device must be clearly
specified on the device.
(5) If the instructions for the operation of the device, or the operating or
adjustment parameters for the device, are displayed by means of a visual
system incorporated into the device, the instructions or parameters must be
able to be understood by the user and, if appropriate, the patient.
12.13 Active implantable medical devices
(1) An active implantable medical device must display a code that can be used
to identify:
(a) the type of device; and
(b) the manufacturer of the device; and
(c) the year of manufacture of the device.
(2) the code must be able to be read without the need for surgery to the person
in whom the device is implanted.

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13. Information supplied by the manufacturer
13.1 Information to be provided with medical devices – general
(1) The following information must be provided with a medical device:
(a) information identifying the device;
(b) information identifying the manufacturer of the device;
(c) information explaining how to use the device safely,
having regard to the training and knowledge of potential users of the
device.
(2) In particular:
(a) the information required by clause 13.3 must be provided with a
medical device; and
(b) if instructions for use of the device are required under subclause 13.4,
the information mentioned in subclause 13.4(3) must be provided in
those instructions.
(3) The information:
(a) must be provided in English; and
(b) may also be provided in any other language.
(4) The format, content and location of the information must be appropriate for
the device and its intended purpose.
(5) Any number, letter, symbol, or letter or number in a symbol, used in the
information must be legible and at least 1 millimetre high.
(6) If a symbol or identification colour that is not included in a medical device
standard is used in the information provided with the device, or in the
instructions for use of the device, the meaning of the symbol or identification
colour must be explained in the information provided with the device or the
instructions for use of the device.

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13.2 Information to be provided with medical devices – location
(1) Unless it is impracticable and inappropriate to do so, the information
required to be provided with a medical device must be provided on the
device itself.
(2) If it is not practicable to comply with subclause (1) in relation to the provision
of the information, the information must be provided:
(a) on the packaging used for the device; or
(b) in the case of devices that are packaged together because individual
packaging of the devices is not practicable – on the outer packaging
used for the devices.
(3) If it is not practicable to comply with subclause (1) or (2) in relation to the
provision of the information under clause 13.3, the information must be
provided on a leaflet supplied with the device.
(4) If it is not practicable to comply with subclause (1) or (2) in relation to the
provision of the information under clause 13.4, the information must be
provided in printed documents or other appropriate media.

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13.3 Information to be provided with medical devices – particular requirements
The information mentioned below must be provided with a medical device.
(1) The manufacturer’s name, or trade name, and address
(2) The intended purpose of the device, the intended user of the device, and
the kind of patient on whom the device is intended to be used where these
are not obvious
(3) Sufficient information to enable a user to identify the device, or if relevant,
the contents of packaging
(4) Any particular handling or storage requirements applying to the device
(5) Any warnings, restrictions on use, or precautions that should be taken, in
relation to the use of the device
(6) Any special operating instructions for the use of the device
(7) If applicable, an indication that the device is intended for a single use only
(8) If applicable, an indication that the device has been custom-made for a
particular individual and is intended for use only by that individual
(9) If applicable, an indication that the device is intended to be used only for
clinical or performance investigations before being supplied
(10) For a sterile device, the word “STERILE” and information about the method
that was used to sterilise the device
(11) The batch code, lot number or serial number of the device.
(12) If applicable, a statement of the date (expressed in a way that clearly
identifies the month and year) up to when the device can be safely used
(13) If the information provided with the device does not include the information
mentioned in item 12 – a statement of the date of manufacture of the device
(this may be included in the batch code, lot number or serial number of the
device provided the date is clearly identifiable)
(14) If applicable, the words “for export only”
Note: In addition to the information mentioned above, regulation 10.2 requires certain
information to be provided with a medical device.

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 Manufacturer: Product: ID:

A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

applied by manufacturer procedures applied by for non- applicability
Only if the manufacturer applied manufacturer This column to contain direct reference to
Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

13.4 Instructions for use
(1) Instructions for the use of a medical device must be provided with the
device.
(2) However, instructions for use of a medical device need not be provided with
the device, or may be abbreviated, if:
(a) the device is a Class I medical device or a Class IIa medical device;
and
(b) the device can be used safely for its intended purpose without
instructions.
(3) Instructions for the use of a medical device must include information
mentioned below that is applicable to the device.
(1) The manufacturer’s name, or trade name, and address
(2) The intended purpose of the device, the intended user of the device,
and the kind of patient on whom the device is intended to be used
(3) Information about any risk arising because of other equipment likely to
be present when the device is being used for its intended purpose (for
example, electrical interference from electro-surgical devices or
magnetic field interference from magnetic resonance images)
(4) Information about the intended performance of the device and any
undesirable side effects caused by use of the device
(5) Any contraindications, warnings, restrictions on use, or precautions
that may apply in relation to use of the device
(6) Sufficient information to enable a user to identify the device, or if
relevant, the contents of the packaging
(7) Any particular handling or storage requirements applying to the device
(8) If applicable, an indication that the device is intended for a single use
only
(9) If applicable, an indication that the device has been custom-made for a
particular individual and is intended for use only by that individual
(10) If applicable, an indication that the device is intended to be used only
for clinical or performance investigations before being supplied.
(11) For a sterile device, the word “STERILE” and information about the
method that was used to sterilise the device
(12) For a device that is intended by the manufacturer to be supplied in a
sterile state:
(a) an indication that the device is sterile; and
(b) information about what to do if sterile packaging is damaged and;
(c) if appropriate, instructions for resterilisation of the device.
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 Manufacturer: Product: ID:

A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

applied by manufacturer procedures applied by for non- applicability
Only if the manufacturer applied manufacturer This column to contain direct reference to
Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

(13) For a medical device that is intended by the manufacturer to be
sterilised before use – instructions for cleaning and sterilising the
device which, if followed, will ensure that the device continues to
comply with the applicable provisions of the essential principles
(14) Any special operating instructions for the use of the device
(15) Information to enable the use to verify whether the device is properly
installed and whether it can be operated safely and correctly, including
details of calibration (if any) needed to ensure that the device operates
properly and safely during its intended life
(16) Information about the nature and frequency of regular and preventative
maintenance of the device, including information about the
replacement of consumable components of the device during its
intended life
(17) Information about any treatment or handling needed before the device
can be used
(18) For a device that is intended by the manufacturer to be installed with,
or connected to, another medical device or other equipment so that the
device can operate as required for its intended purpose – sufficient
information about the device to enable the user to identify the
appropriate other medical device or equipment that will ensure a safe
combination.
(19) For an implantable device – information about any risks associated
with its implantation
(20) For a reusable device:
(a) information about the appropriate processes to allow reuse of the
device (including information about cleaning, disinfection, packaging,
and, if appropriate, resterilisation of the device); and
(b) an indication of the number of times the device may be safely
reused.
(21) For a medical device that is intended by the manufacturer to emit
radiation for medical purposes – details of the nature, type, intensity
and distribution of the radiation emitted
(22) Information about precautions that should be taken by a patient and
the user if the performance of the device changes
(23) Information about precautions that should be taken by a patient and
the user if it is reasonably foreseeable that use of the device will result
in the patient or user being exposed to adverse environmental
conditions

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 Manufacturer: Product: ID:

A/NA * Medical Device Standards Other standards or Evidence of compliance or reason

applied by manufacturer procedures applied by for non- applicability
Only if the manufacturer applied manufacturer This column to contain direct reference to
Medical Devices Essential Principles Checklist standards published as Medical EN; ISO; international , local documents such as: study results, test
Device Standard Orders or Conformity standards or company reports, design outputs identified by number /
Assessment Standard Order by the procedures identified by title within the Quality System.
TGA number / title.

* APPLICABLE OR NOT TO THE DEVICE – IF NOT APPLICABLE JUSTIFICATION IS TO BE INCLUDED

(24) Adequate information about any medicinal product that the device is
designed to administer, including and limitations on the substances t
hat may be administered using the device
(25) Information about any medicine (including any stable derivative of
human blood or blood plasma) that is incorporated, or intended to be
incorporated, into the device as an integral part of the device.
(26) Information about precautions that should be taken by a patient and
the user if there are special or unusual risks associated with the
disposal of the device
(27) Information about the degree of accuracy claimed if the device has a
measuring function
(28) Information about any particular facilities required for use of the device
or any particular training or qualifications required by the user of the
device.
14. Clinical evidence

Every medical device requires clinical evidence, appropriate for the use and
classification of the device, demonstrating that the device complies with the
applicable provisions of the essential principles.
Note: See regulation 3.11 and the clinical evaluation procedures.

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