This document specifies general test methods for rotary instruments used in dentistry. These test methods are used for measuring the dimensional characteristics, neck strength and surface roughness of rotary instruments, such as burs, cutters, polishers, grinding instruments and rotary instruments used for oral surgery such as drills and countersinks.
Specific tests are specified in the respective instrument standards, if available.
This document does not specify test methods for materials used for rotary instruments.
NOTE       For materials used for rotary instruments, see ISO 21850-1 and respective instrument standards.
This document is not applicable to endodontic instruments. For endodontic instruments, see ISO 3630-1.

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This document specifies the requirements for enlargers not cited in ISO 3630-1, ISO 3630-3, ISO 3630-4, ISO 3630-5, ISO TR 3630-6 or ISO 3630-7.
This document specifies the requirements for size, marking, product designation, safety considerations, and labelling and packaging, including the instructions for use.

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This document specifies requirements and test methods for stationary dental units concerning
a) the properties of stationary dental unit connections to the compressed air supply, water supply,
suction supply, and wastewater drain plumbing,
b) the materials, design, and construction of the compressed air and water system within the
stationary dental unit,
c) the quality for incoming water and air,
d) the performance of stationary dental unit suction system, and
e) the air, water, suction and wastewater properties of stationary dental unit connections to the
interfaces to dental handpieces.
This document also specifies requirements for instructions for use and technical description.
This document does not specify requirements or test methods for the effectiveness of stationary dental
unit waterline biofilm control.
NOTE Test methods for the effectiveness of stationary dental unit waterline biofilm control are specified in
ISO 16954.
This document is only applicable to stationary dental units that are not used for oral surgery treatment
requiring sterile air and water supplies. Amalgam separators are not included in this document.

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This document specifies requirements and test methods for stationary dental units concerning
a) the properties of stationary dental unit connections to the compressed air supply, water supply, suction supply, and wastewater drain plumbing,
b) the materials, design, and construction of the compressed air and water system within the stationary dental unit,
c) the quality for incoming water and air,
d) the performance of stationary dental unit suction system, and
e) the air, water, suction and wastewater properties of stationary dental unit connections to the interfaces to dental handpieces.
This document also specifies requirements for instructions for use and technical description.
This document does not specify requirements or test methods for the effectiveness of stationary dental unit waterline biofilm control.
NOTE       Test methods for the effectiveness of stationary dental unit waterline biofilm control are specified in ISO 16954.
This document is only applicable to stationary dental units that are not used for oral surgery treatment requiring sterile air and water supplies. Amalgam separators are not included in this document.

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This document specifies the general requirements and test methods for diamond rotary instruments
used in dentistry, including designation, colour code and grit sizes and a quality control for these
instruments.
It applies to all types of diamond rotary instruments independent of type and shape with exception to
diamond discs, which are specified in ISO 7711-2.

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This document specifies requirements and their test methods for tissue punches used with a handpiece in dentistry especially for oral surgical implant procedures, such as cutting holes or notches in and removing of gingival tissue. It also specifies the requirements for their marking and labelling.

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This document specifies dimensions and performance requirements for excavators used in dentistry.

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This document specifies the requirements and test methods for endodontic compactors (pluggers and
spreaders) which are used for the compaction of endodontic filling materials, and also heat-carriers
(which are not specified in the other parts of the ISO 3630 series).
This document specifies the requirements for size, marking, product designation, safety considerations,
and their labelling and packaging.

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This document specifies dimensions and performance requirements for excavators used in dentistry.

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This document specifies requirements and their test methods for tissue punches used with a handpiece in dentistry especially for oral surgical implant procedures such as cutting holes or notches in and removing of gingival tissue. It also specifies the requirements for their marking and labelling.

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This document specifies requirements and their test methods for tissue punches used with a handpiece in dentistry especially for oral surgical implant procedures, such as cutting holes or notches in and removing of gingival tissue. It also specifies the requirements for their marking and labelling.

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This document specifies dimensions and performance requirements for excavators used in dentistry.

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This document specifies requirements and test methods for hand-held and mechanically operated instruments used for shaping and cleaning root canals, and which are not specified in other parts of the ISO 3630 series.
This document specifies requirements for size, marking, product designation, safety considerations, labelling and packaging.

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This document specifies requirements, test methods, instructions for use and marking for multifunction handpieces (colloquially called "syringes") intended to be used in the oral cavity of the patient.
This document does not apply to dental handpieces and motors, intraoral cameras, dental polymerisation lamps, powered scalers, powder jet handpieces, prophy handpieces, suction cannulas and saliva ejectors.

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This document specifies requirements and test methods for hand-held and mechanically operated
instruments used for shaping and cleaning root canals, and which are not specified in other parts of the
ISO 3630 series.
This document specifies requirements for size, marking, product designation, safety considerations,
labelling and packaging.

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This document specifies general requirements and test methods for metallic dental tweezers of the Meriam type and for College type.
This document is not applicable to anatomical tweezers and surgical tweezers.

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This document is one of a series of standards describing the characteristics for identification cards as defined in the definitions clause and the use of such cards for international interchange.
This document specifies requirements for a high coercivity magnetic stripe (including any protective overlay) on an identification card and encoding technique. It takes into consideration both human and machine aspects and states minimum requirements.
Coercivity influences many of the quantities specified in this document but is not itself specified. The main characteristic of the high coercivity magnetic stripe is its improved resistance to erasure. This is achieved with minimal probability of damage to other magnetic stripes by contact while retaining read compatibility with magnetic stripes as defined in ISO/IEC 7811-2.
This document provides for a card capacity of approximately 10 times that of a card conforming to ISO/IEC 7811-6. The number of tracks has been increased to 6, each track being approximately half the width of tracks conforming to ISO/IEC 7811-6, located so that readers designed to read these high density tracks will also be able to read cards conforming to ISO/IEC 7811-2 and ISO/IEC 7811-6. Data is encoded in 8 bit bytes using the MFM encoding technique. Data framing is used to limit error propagation and error correction techniques further improve reliability of reading.
It is the purpose of the ISO/IEC 7811 series of standards to provide criteria to which cards shall perform. No consideration is given within these standards to the amount of use, if any, experienced by the card prior to test. Failure to conform to specified criteria is negotiated between the involved parties.
ISO/IEC 10373-2 specifies the test procedures used to check cards against the parameters specified in this document.
NOTE Numeric values in the SI and/or Imperial measurement system in this document may have been rounded off and are consistent with, but not exactly equal to each other. Using either system is correct but intermixing or reconverting values can result in errors. The original design was made using the Imperial measurement system.

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This document specifies requirements and their test methods for stainless steels used in
dental instruments.
It is applicable to single-use and reusable instruments, regardless of whether they are connected to a
power-driven system or not.
It contains a current selection of stainless steels suitable for use in the manufacture of dental
instruments.

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This document specifies requirements, test methods, instructions for use and marking for multifunction handpieces (colloquially called "syringes") intended to be used in the oral cavity of the patient. This document does not apply to dental handpieces and motors, intraoral cameras, dental polymerisation lamps, powered scalers, powder jet handpieces, prophy handpieces, suction cannulas and saliva ejectors.

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This document specifies general requirements and test methods for endodontic instruments used for endodontic purposes, e.g. enlargers, compactors, accessory instruments, shaping and cleaning instruments, and a numeric coding system. In addition, it covers general size designations, color-coding, packaging, and identification symbols.

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2019-01-21: Parallel process missed, so adoption of published ISO

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EN-ISO 7782-2 specifies dimensional and other requirements for the 11 most commonly used carbide cutters which are predominantly used in the dental laboratory.

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This document specifies general requirements and test methods for endodontic instruments used for endodontic purposes, e.g. enlargers, compactors, accessory instruments, shaping and cleaning instruments, and a numeric coding system. In addition, it covers general size designations, color-coding, packaging, and identification symbols.

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This document specifies requirements and test methods for reusable intra-oral mirrors with a coated
glass reflecting surface used for dental purposes in the oral cavity.
In addition, specific requirements for metallic casing and metallic handles are given.

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ISO 9687:2015 specifies graphical symbols for dental equipment. It is intended that the symbols are to be used on the appropriate piece of dental equipment and in documents pertaining to dental equipment, for example in instructions for use, marking, labelling, and technical product documentation.

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ISO 21533:2018 specifies requirements and test methods for reprocessable cartridge syringes intended for intraligamentary injections.
ISO 21533:2018 specifies requirements for cartridge syringes with ISO metric thread sizes, and only intended for intraligamentary injections. However, attention is drawn to the existence of a variety of syringes with imperial thread sizes (see Annex A).

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ISO 14457:2017 specifies requirements and test methods for handpieces and motors used in dentistry for treatment of patients and having patient contact, regardless of their construction. It also specifies requirements for manufacturer's information, marking and packaging.
ISO 14457:2017 is applicable to the following:
a)    straight and angle handpieces;
b)    high-speed air turbine handpieces;
c)    air motors;
d)    electrical motors;
e)    prophy handpieces.
ISO 14457:2017 is not applicable to the following:
-      intraoral camera handpieces;
-      powered polymerization handpieces;
-      air-powered scalers;
-      electrical-powered scalers;
-      powder jet handpieces;
-      multifunction handpieces (syringes).
NOTE       See Annex A for clarification of handpieces and motor types covered by ISO 14457:2017.

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This document specifies requirements and test methods for handpieces and motors used in dentistry
for treatment of patients and having patient contact, regardless of their construction. It also specifies
requirements for manufacturer’s information, marking and packaging.
This document is applicable to the following:
a) straight and angle handpieces;
b) high-speed air turbine handpieces;
c) air motors;
d) electrical motors;
e) prophy handpieces.
This document is not applicable to the following:
— intraoral camera handpieces;
— powered polymerization handpieces;
— air-powered scalers;
— electrical-powered scalers;
— powder jet handpieces;
— multifunction handpieces (syringes).
NOTE See Annex A for clarification of handpieces and motor types covered by this document.

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ISO 19490:2017 specifies requirements and their test methods for sinus membrane elevators used during the placement of dental implants for sinus floor lifting. It also specifies the requirements for their marking and labelling.

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ISO 1797:2017 specifies the requirements for dimensions and material properties of shanks used in dentistry for rotary or oscillating instruments. It describes the measurement methods for the verification of the requirements.
ISO 1797:2017 is not applicable to tips fixed to the handpiece with a screw, e.g. scaler tips.
Information about the location of marking is also given. Annex A on quality control is included in order to ensure a high quality level.

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ISO 7787-3:2017 specifies dimensional and other requirements for the three most commonly used carbide cutters for milling machines which are predominantly used in the dental laboratory.
Other characteristics of laboratory cutters (for example, spiralled blades or cross-cut) are not covered by this document.
Cutters intended for use with CAD/CAM systems are excluded from the scope of this document.

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ISO 19715:2017 specifies requirements and test methods for a filling instrument with contra angle, which is used for the restoration of teeth via the application of polymer-based restorative materials and cements. It also specifies requirements for the design, dimensions and marking.

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ISO 14457:2017 specifies requirements and test methods for handpieces and motors used in dentistry for treatment of patients and having patient contact, regardless of their construction. It also specifies requirements for manufacturer's information, marking and packaging. ISO 14457:2017 is applicable to the following: a) straight and angle handpieces; b) high-speed air turbine handpieces; c) air motors; d) electrical motors; e) prophy handpieces. ISO 14457:2017 is not applicable to the following: - intraoral camera handpieces; - powered polymerization handpieces; - air-powered scalers; - electrical-powered scalers; - powder jet handpieces; - multifunction handpieces (syringes). NOTE See Annex A for clarification of handpieces and motor types covered by ISO 14457:2017.

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This International Standard specifies requirements and their test methods for sinus elevator used in dentistry especially for lateral approach of sinus floor elevation. It also specifies the requirements for their marking and labelling.

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This International Standard specifies requirements and test methods for filling instruments with working ends with contra set, used for the restoration of teeth with plastic filling materials. It also specifies requirements for their design, dimensions and marking.

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This document specifies dimensional and other requirements for the three most commonly used
carbide cutters for milling machines which are predominantly used in the dental laboratory.
Other characteristics of laboratory cutters (for example, spiralled blades or cross-cut) are not covered
by this document.
Cutters intended for use with CAD/CAM systems are excluded from the scope of this document.

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This document specifies the requirements for dimensions and material properties of shanks used
in dentistry for rotary or oscillating instruments. It describes the measurement methods for the
verification of the requirements.
This document is not applicable to tips fixed to the handpiece with a screw, e.g. scaler tips.
Information about the location of marking is also given. Annex A on quality control is included in order
to ensure a high quality level.

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ISO 3964:2016 specifies the coupling between handpieces and motors connected to dental units.
ISO 3964:2016 specifies the nominal dimensions, tolerances and the extraction force of coupling systems for use between handpiece and motor which supply the handpiece with water, air and light and rotation energy.

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ISO 9173-1:2016 specifies the general performance requirements for extraction forceps used in dentistry.

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ISO 19490:2017 specifies requirements and their test methods for sinus membrane elevators used during the placement of dental implants for sinus floor lifting. It also specifies the requirements for their marking and labelling.

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ISO 17509:2016 specifies requirements for torque transmitters to be used in oral implantology in conjunction with a dental handpiece as an accessory in the placement of dental implants and the further manipulation of connecting parts in the craniofacial area.
ISO 17509:2016 applies to torque transmitters used for placement and for removal in the oral cavity of the patient which are connected to power-driven systems having torque control mechanism, but does not apply to the power-driven systems themselves.
ISO 17509:2016 does not include the dental implant nor parts that would be connected to it.
With regard to safety, this International Standard gives requirements for classification, intended performance, performance attributes, material selection, performance evaluation, manufacture, reprocessing and information to be supplied by the manufacturer.

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ISO 2157:2016 specifies the nominal diameters of the working parts of dental rotary instruments, for example burs, laboratory burs, grinding instruments, diamond instruments, mandrels and the corresponding designation.
Excluded are the diameters of endodontic instruments and scaler tips.

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ISO 7787-1:2016 specifies dimensional and other requirements for the nine most commonly used steel cutters which are predominantly used in the dental laboratory.
Other characteristics of laboratory cutters, for example, spiralled blades or cross-cut, are not covered by this part of ISO 7787.
NOTE          These cutters are also used in podiatry.

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ISO 18556:2016 specifies requirements and their test methods for metallic and non-metallic intraoral spatulas used to introduce and model filling materials into a tooth cavity, including single use disposable items.
NOTE          This includes instruments used for placement and contouring of non-metallic direct restorative materials.
It also specifies requirements for their marking and labelling.

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This International Standard determines a degree of firing to be implemented by the user. It represents a test method for
adapting the firing program of a dental furnace by determining the degree of firing of fired test specimens for a dental
ceramic.
The test method is suitable for powdered dental ceramics according to ISO 6872, Type I.
The test method enables monitoring of the temperature control in the dental furnace by evaluating the firing degree of a
dental ceramic. The test method is also suitable for evaluating the reproducibility of the firings in a dental furnace or for
comparing several dental furnaces.

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ISO 18397:2016 specifies requirements and test methods for air-powered and electrical-powered scaler handpieces and scaler tips, including piezo, ferrostrictive and magnetostrictive type ultrasonic scalers, operated as stand-alone items or connected to dental units, for use on patients. It also contains specifications on manufacturers' instructions, marking and packaging.

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This International Standard specifies the nominal diameters of the working parts of dental rotary
instruments, for example burs, laboratory burs, grinding instruments, diamond instruments, mandrels
and the corresponding designation.
Excluded are the diameters of endodontic instruments and scaler tips.

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This International Standard specifies requirements and test methods for air-powered and electricalpowered
scaler handpieces and scaler tips, including piezo, ferrostrictive and magnetostrictive type
ultrasonic scalers, operated as stand-alone items or connected to dental units, for use on patients. It
also contains specifications on manufacturers’ instructions, marking and packaging.

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ISO 17937:2015 specifies requirements and their test methods for osteotomes used in dentistry for bone compaction, internal sinus floor elevation, and jaw bone cleaving. It also specifies the requirements for their marking and labelling.

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ISO 13397-5:2015 specifies the designs and dimensions for Jacquette scalers.

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