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IEC specifications device retail

IEC specifications device retail

IEC provides a standardized approach to testing and certification. IEC testing brings together the agreed upon set of rules, specifications, and terminology that allow manufacturers to have their devices tested for conformity. Testing a product or device to a Standard then allows that one assessment to provide access to several markets.

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  • IEC Testing Certification - IEC Compliance Standards

    IEC provides a standardized approach to testing and certification. IEC testing brings together the agreed upon set of rules, specifications, and terminology that allow manufacturers to have their devices tested for conformity. Testing a product or device to a Standard then allows that one assessment to provide access to several markets.

    Get Price
  • IEC 60601: Product Safety Standards for Medical Devices

    IEC 60601: Product Safety Standards for Medical Devices. IEC 60601 is a widely accepted series of international standards for the basic safety and essential performance of medical electrical equipment. Your new and existing medical devices must demonstrate compliance with the latest revision of IEC 60601.

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  • IEC 62047 Series - Micro-Electromechanical Devices - MEMS

    The IEC 62047 series of semiconductor standards concerns itself with micro-electromechanical devices, also known as MEMS. This 22 standard series starts from the basics with terms, definitions, and general specs, and continues on to a range of measurements and test methods such as those for fatigue, compression, bending, and shearing.

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  • ISO - IEC 62366-1:2015 - Medical devices — Part 1

    IEC 62366-1:2015 specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY of a MEDICAL DEVICE as it relates to SAFETY. This USABILITY ENGINEERING (HUMAN FACTORS ENGINEERING) PROCESS permits the MANUFACTURER to assess and mitigate RISKS associated with CORRECT USE and USE ERRORS, i.e., NORMAL USE.

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  • Medical Device Testing - IEC 60601, IEC 61010 | Eurofins EE

    Eurofins Electrical and Industrial laboratories offer accredited Medical device testing for EN/IEC 60601 EN/IEC 61010 series for medical electrical equipment under the Medical Devices Directive (MDD) 93/42/EEC and In Vitro Diagnostics Devices Directive (IVDD) 98/79/EC approvals.

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  • NEMA and IEC schematic diagram comparisons -

    IEC schematic diagrams General With the increasing emphasis on globalization, many industries are now looking to all parts of the world to produce, market, and sell their products. Electrical manufacturers are no exception. Since the electrical standards adopted

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  • Medical Device Software Standards for Safety and

    3 IEC 62304 background Specifically created for medical device software IEC 60601-1-4 and general software engineering standards were not considered adequate Significant FDA involvement from start Scope includes “stand-alone software” and “embedded software” Based on ANSI/AAMI/SW68 with a few significant differences Omits requirements duplicated elsewhere (QMS)

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  • UnifiedPOS | Object Management Group

    UnifiedPOS is an architectural specification for application interfaces to point-of-service devices that are used in a retail environment. This standard helps ensure that when device drivers are designed according to the specification, devices can be changed or added to the mix at the point of sale (POS) with a minimum of programming work to make them function properly, regardless of operating

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  • Which type of residual current device (RCD) you should use

    Sep 09, 2020Type B for RCDs is not mentioned in these reference standards: an international standard, IEC 62423, has been introduced in 2007, specifying additional requirements for type B RCDs. This new standard, IEC 62423 , should only be referred to together with IEC 61008-1 (for RCCBs) and IEC 61009-1 (for RCD-blocks and RCBOs), this means that B type

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  • Class 4 laser safety requirements: what you need to know

    May 15, 2018Typically, in the United States, safety guidance is coming from ANSI Z136 standards (American Standard Institute). The LIA (Laser Institute of America) being the publisher of those standards. Class 4 is currently the most dangerous class, with lasers in this category being able to cause severe injuries for the skin and eyes.

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  • How to Configure a Point of Sale in D365 for Retail in a

    Retail Channel setup POS setup Devices. One of the last steps we will initiate is the activation of our POS that will enable us to begin executing transactions for our retail entity. We will use device Houston-14 as shown in Fig 14 to activate, as this is the one we set up as a Retail Cloud POS.

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  • PanelView 5310 Terminals Specifications

    The PanelView™ 5310 terminals are operator interface devices that monitor and control devices attached to ControlLogix 5570 and 5580, and CompactLogix™ L1, L2, and L3 controllers over an EtherNet/IP™ network. Animated graphic and text displays provide operators with a view into the operating state of a machine or process.

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  • Safety Integrity Level (SIL) - 61508/61511

    Electric and electronic devices can be certified for use in functional safety applications according to IEC 61508, providing application developers the evidence required to demonstrate that the application including the device is also compliant. IEC 61511 is an application specific adaptation of IEC 61508 for the Process Industry sector.

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  • Standards: Medical Devices - UW Bioengineering

    Standards: Medical Devices Medical devices are subject to strict general controls and procedural regulations. The development and use of standards is vital to ensuring the safety and efficacy of medical devices. Standardization (ISO), International Electrotechnical Commission (IEC), and ASTM International, formally

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