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ANSI B11.19-2019

Performance Requirements for Risk Reduction Measures: Safeguarding and other Means of Reducing Risk

This standard provides performance requirements for the design, construction, installation, operation, and maintenance of the risk reduction measures listed below when applied to machines -inherently safe by design (see clause 7); engineering controls – guards (see clause 8); engineering controls – control functions (see clause 9); engineering controls – devices (see clause 10); administrative controls (see clause 11).


ASTM F2100-19

Standard Specification for Performance of Materials Used in Medical Face Masks

1.1 This specification covers testing and requirements for materials used in the construction of medical face masks that are used in providing healthcare services such as surgery and patient care. 1.2 This specification provides for the classification of medical face mask material performance. Medical face mask material performance is based on testing for bacterial filtration efficiency, differential pressure, sub-micron particulate filtration efficiency, resistance to penetration by synthetic blood, and flammability. 1.3 This specification does not address all aspects of medical face mask design and performance. This specification does not specifically evaluate the effectiveness of medical face mask designs as related to the barrier and breathability properties. This specification does not apply to regulated respiratory protection, which may be necessary for some healthcare services. 1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.5 The following precautionary caveat pertains only to the test methods portion, Section 9 , of this specification: This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.


ANSI/ESD S20.20-2014

Protection of Electrical and Electronic Parts, Assemblies and Equipment (Excluding Electrically Initiated Explosive Devices)

This standard provides administrative and technical requirements for establishing, implementing, and maintaining an ESD Control Program to protect electrical or electronic parts, assemblies, and equipment susceptible to damage by electrostatic discharges greater than or equal to 100 volts HBM, 200 volts CDM, and 35 volts on isolated conductors.


ANSI/ISEA Z87.1-2015

American National Standard for Occupational and Educational Personal Eye and Face Protection Devices

This standard sets forth criteria related to the general requirements, testing, permanent marking, selection, care, and use of protectors to minimize the occurrence and severity or prevention of injuries from such hazards as impact, non-ionizing radiation and liquid splash exposures in occupational and educational environments including, but not limited to, machinery operations, material welding and cutting, chemical handling, and assembly operations. Certain hazardous exposures are not covered in this standard. These include, but are not limited to: Bloodborne pathogens, X-rays, high energy particulate radiation, microwaves, radio-frequency radiation lasers, masers, and sports and recreation.


ANSI/ISEA Z358.1-2014

American National Standard for Emergency Eyewash and Shower Equipment

This standard establishes minimum performance and use requirements for eyewash and shower equipment for the emergency treatment of the eyes or body of a person who has been exposed to hazardous materials. It covers the following types of equipment: emergency showers, eyewashes, eye/face washes, and combination units. This standard also includes performance and use requirements for personal wash units and drench hoses, which are considered supplemental to emergency eyewash and shower equipment.


ISO 9001:2015

Quality management systems - Requirements

ISO 9001:2015 specifies requirements for a quality management system when an organization: a) needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and b) aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements. All the requirements of ISO 9001:2015 are generic and are intended to be applicable to any organization, regardless of its type or size, or the products and services it provides.

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ISO 14971:2019

Medical devices - Application of risk management to medical devices

This document specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process described in this document intends to assist manufacturers of medical devices to identify the hazards associated with the medical device, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls. The requirements of this document are applicable to all phases of the life cycle of a medical device. The process described in this document applies to risks associated with a medical device, such as risks related to biocompatibility, data and systems security, electricity, moving parts, radiation, and usability. The process described in this document can also be applied to products that are not necessarily medical devices in some jurisdictions and can also be used by others involved in the medical device life cycle. This document does not apply to: — decisions on the use of a medical device in the context of any particular clinical procedure; or — business risk management. This document requires manufacturers to establish objective criteria for risk acceptability but does not specify acceptable risk levels. Risk management can be an integral part of a quality management system. However, this document does not require the manufacturer to have a quality management system in place. NOTE Guidance on the application of this document can be found in ISO/TR 24971.



ANSI/SAIA A92.22 – 2018

Safe Use of Mobile Elevating Work Platforms (MEWPs)

Scope: This American National Standard specifies requirements for application, inspection, training, maintenance, repair and safe operation of Mobile Elevating Work Platforms (hereafter known as MEWPs). It applies to all types and sizes of MEWPs as specified in ANSI/SAIA A92.20 (design, calculations, safety requirements and test methods) that are intended to position personnel, along with their necessary tools and materials, at work locations.


ANSI/SAIA A92.24 – 2018

Training Requirements for the Use, Operation, Inspection, Testing and Maintenance of Mobile Elevating Work Platforms (MEWPs)

Scope: This standard provides methods and guidelines to prepare MEWP training materials, defines administrative criteria, and delivers elements required for proper training and familiarization. It applies to all types and sizes of MEWPs defined in ANSI/SAIA A92.20 (design, calculations, safety requirements and test methods) that are intended to position personnel, along with their necessary tools and materials, at work locations.


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As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

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