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dilo device IEC specifications deivces

dilo device IEC specifications deivces

The Mini Series features devices perfectly suited for gas handling of small gas compartments and gas reclaiming to < 5 mbar. This series even exceeds the IEC standards and can compete with the more powerful series. We recommend using this series for small gas quantities. Oil free compressors allow gas handling without contamination by oil residues.

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  • IEC specifications for SF6 gas - DILO

    Relevant IEC specifications/norms for SF6 gas are: IEC 60376 for new gas, IEC 60480 for used SF6 gas and IEC 62271-4 as SF6 reuse specification.

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  • SF6 gas moisture measuring device - DILO

    Electronic moisture measuring device with dew point indication For determination of moisture. 3-037-R001 . Moisture is the most important criteria for the determination of the gas quality.

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  • Portable SF6 gas refilling device - DILO

    SF 6 gas refilling device For reliable refilling of SF 6 gas by overpressure. 3-393-R001 SF 6 gas refilling device for high voltage Portable with rubber hose and couplings DN8 and DN20, Pressure range 0 up to 10 bar. 3-393-R002 SF 6 gas refilling device for high voltage Portable in a case with rubber hose and couplings DN8 and DN20, Pressure range 0 up to 10 bar

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  • DILO Multi-Analyser SF6 - check of SF6 gas quality

    The MultiAnalyser SF6 allows different methods of operation for emission-free handling of the measured gas: » Internal storage of the measured gas (max. inlet pressure 35 bar pe) within the device, in an external cylinder or an external gas collecting bag.

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  • DILO Company, Inc. | World Leader in SF6 Maintenance Equipment

    If you're looking for a SF6 gas handling specialist that combines quality, innovation, and sustainability with excellent customer service, then DILO is for you. For over 50 years, customers around the world have valued DILO as an important partner for professional and emission-free SF6 gas handling.

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  • AFTER SALES - DILO Company, Inc. | Dilo Company, Inc

    DILO Company, Inc. 11642 Pyramid Drive Odessa, FL 33556 Phone: 727-376-5593 E-Mail: [email protected]

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  • Return of DILO devices | DILO GmbH

    Return of DILO devices. Before returning your Dilo equipment to us, we request that you inform us if the materials/substance you have been using in the equipment are hazardous. The reason for this request of information is necessary for the safety of our technicians. They must have prior knowledge of what has been used so as they can apply the

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  • IEC specifications device with return system

    IEC specifications device with return system. Software has become the key differentiator for manufacturers of medical devices. There are countless opportunities for software innovation, but are counterbalanced by stringent quality requirements, risks of product failure, and growing regulatory complexities.

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  • IEC Standards vs. Performance Standards for Medical Devices

    1 IEC Standards vs. Performance Standards for Medical Devices Robert Sauer, M.S. Office of In Vitro Diagnostics Radiological Health . Center for Devices and Radiological Health

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  • IEC specifications purification device with return system

    Electrotechnical Commission (IEC) standards: IEC 61000-4-2, IEC 61000-4-4, and IEC 61000-4-5. We will begin with: 1. A brief review of EMI, EFT, and ESD specifications. 2. Key ESD protection device specifications definitions. 3. A quick summary of EMI, EFT, and ESD protection strategies. 4. Capacitor filter selection and characteristics. 5. Get

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  • SF6 gas handling - DILO

    DILO supplies the measuring devices required for the directive. However, DILO separating units allow the SF 6 gas mixture to be purified to the extent that it even meets the standards of IEC 60376 a transport pressure reduction with pressure equalisation generally needs to be carried out in the device. Most DILO devices are equipped

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  • IEC specifications purification device for Light Rail

    IEC specifications purification device for Light Rail. en 50126 (iec 62278), en 50129 (iec 62425), en 50128 (iec 62279) and en 50159. Target group of the EN 5012x training The training targets developers, testers, project leads, quality representatives and safety officers primarily focusing on the development of programmable electronic safety systems; users and integrators of safety devices

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  • DILO Moisture Measuring Device | Determine SF6 Quality

    3-037-R002. Moisture is the most important criteria for the determination of the gas quality. This device has been designed specifically for SF 6 moisture measurements. It shows a higher resistance against contamination and SF 6 decomposition products than conventional moisture sensors and even minimizes the usual long-time drift.

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  • PDF List of Recognized Standards for Medical Devices

    Medical devices - Application of risk management to medical devices IEC 61010‐1:2001‐Ed.2.0 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements IEC 61010‐1/Cor.1:2002 IEC 61010‐1/Cor.2:2003 IEC 61010‐2‐101:2002‐Ed.1.0

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  • International | DILO GmbH

    The IEC requirements are exceeded by far when using DILO devices as DILO service carts enable a final vacuum of < 1 mbar depending on the type of device. IEC 60480:2019 guideline This guideline stipulates the limit values for the re-use of SF 6 gas in medium and high voltage switchgear.

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  • Medical Device Marking and Labeling Regulations

    In a global marketplace, harmonization of graphic symbols eases the language barriers and lessens the potential for device misuse. A review of IEC 60601-1's global regulatory importance, A Primer for IEC 60601-1, was presented in an earlier article on MD+DI, and the differences between national standards were discussed in National Deviations to IEC 60601-1.

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  • Services | DILO GmbH

    DILO Armaturen und Anlagen GmbH Frundsbergstrasse 36 D-87727 Babenhausen/Schwaben Tel: +49 (0) 83 33 - 302-0 E-Mail: [email protected]

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  • Online registration of SF 6 devices | DILO GmbH

    Online device registration Your involvement in our aftersales management. Online device registration and benefit immediately. Thank you for purchasing a DILO device. Please use this online form to register your device and get a free guarantee extension of 12 months.

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  • List of Current Medical Device Standards and Collateral

    List of Current Medical Device Standards and Collateral Standards - D.L.S. Electronic Systems, Inc. The table below lists all of the IEC/EN standards for particular types of medical equipment. The standards are used in conjunction with the basic standard IEC 60601-1 and follow the same clause numbering system.

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  • Mini Series: Small SF6 Gas Handling Devices - us.dilo.com

    The Mini Series features devices perfectly suited for gas handling of small gas compartments and gas reclaiming to < 5 mbar. This series even exceeds the IEC standards and can compete with the more powerful series. We recommend using this series for small gas quantities. Oil free compressors allow gas handling without contamination by oil residues.

    Get Price
  • Medical device cyber security testing and assessment

    We have extensive experience of conducting testing on a wide range of networked medical devices. Our assessments are based on IEC 62443-4-2, UL-2900-2-1 (based on UL-2900-1), a TÜV SÜD internal checklist and the FDA guidance; thus aiding your compliance to regulations and access to global markets.

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  • SF6 Gas Monitor and Leak Detector with NDIR - DILO

    The Portable SF 6 Gas Monitor and Leak Detector is an advanced personal gas monitor that uses long-life non-dispersive infrared (NDIR) sensor technology for analyzing and checking low-level gas concentrations in the ambient environment. With very fast response and clearing times, the unit can identify and pinpoint very small levels of sulfur

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  • FDA Software Guidances and the IEC 62304 Software Standard

    The IEC 62304 medical device software standard (Medical device software—Software life cycle processes) is comprised of five processes in five chapters (5-9): 5 - Software Development Process = this is the main process that SW groups are focused on and includes all the key aspects of development from planning and requirements to

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  • ISO and IEC standards for software in medical devices in a

    To have a global view of medical devices with software, people should know 5 standards: ISO 13485 and ISO 14971 on one side, IEC 62304, ISO 60601-1 and IEC 62366, on the other side. The table below summarises the standards around software for medical devices and the responsibilities of people, from the point of view of a software project manager.

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  • IEC 60601-1 Medical Design Standards for Power Supplies

    Figure 1: The shift to IEC 60601-1-2 4th edition standards for medical devices has significant implications for medical device design 2nd Edition - Patient Focus. The intrinsic nature of an ac-dc power supply or a dc-dc converter means the voltages and currents they provide can potentially be hazardous if not properly managed.

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  • EMC for Medical Devices: EN/IEC 60601-1-2, 4th Edition

    The fourth edition IEC/EN 60601-1-2 (4th Edition) will become a mandatory standard covering safety for medical devices on December 31, 2018.1,2 As with any new standard edition, there are changes that necessitate additional evaluations of the product beyond those required by the previous edition. Although emission and immunity tests for medical products are very similar to those applied to

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  • PCB Standards for the Design of Medical Electronic Devices

    F. Ensure that your product meets the standards of IEC 60601 or IEC 61010 depending on its operating environment. Incorporating the above standards into the design of your medical electronic devices will assist you in developing high-quality, reliable products for the medical device industry.

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  • IEC 62366-1 and Usability engineering for software

    It is supported by the publication AAMI HE75 standard, FDA guidances, and the publication of IEC 62366 in 2008 followed by IEC 62366-1:2015. Although usability engineering is a requirement for the design of medical devices, most of people designing software are not familiar with this process. This article is an application of the process

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  • IEC 60601-1 Clause 4.4 Service Life — MEDTEQ

    IEC 60601-1 Clause 4.4 simply asks that this is stated in risk management file. And, having declared this lifetime, the manufacturer must then go on to show that risks are acceptable over the life of the device. For some medical devices, lifetime will be an important factor in many risk related decisions, such as sterility, mechanical wear and

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