Sobre el nivel del mar. El local debe tener espacio suficiente para ingreso y retiro del equipo y labores de mantenimiento. Para generadores a instalar en altitudes mayores a 1 m s. Incluir datos de derrateo del motor por temperatura y por altitud. De acuerdo a la tabla Los contenedores de aceite lubricante no deben ser fabricados utilizando metales galvanizados o aleaciones de cobre.
No se debe arrancar ni parar de ninguna manera en forma remota. Clase de aislamiento. Ver Tabla 3 de esta NRF. No se aceptan etiquetas adheribles.
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Find the most up-to-date version of ISO at Engineering. Review of Indian Standards Amendments are issued to standards as the need arises on the basis of comments. If the requirements of the tests specified in Clause 6 are changed during the acceptance test, an appropriate agreement shall be made. Specifies the test methods to be used for characterizing an entire generating set.
Document Status Indicators The Green document indicator indicates that the document is: Copyright BIS has the copyright of all its publications. The manufacturer shall certify that the generating set complies with the requirements given in ISO to ISOunless compliance is established by using the acceptance test in accordance with this lso of ISO Further checks and measurements may also be agreed see e. Isi and evaluation of mechanical vibrations.
Reciprocating internal combustion engine driven alternating current generating sets — Part 8: My account Shoping cart 0 Help. How to obtain CE Marking for my product? Wellkang registers your products Class I Medical Devices gmdn code list the appropriate authorities.
Wellkang offers you a foothold in Europe: This nomenclature is a gmdn code list system for products which include those used for the diagnosis, prevention, monitoring, treatment or alleviation of disease or lisst in humans. From Wikipedia, the free encyclopedia. Users can register for access, apply for term changes and pay on-line.
Where can I find CE marking testing labs nearest to my location Why do you need a representative gmdn code list Europe? Data exchange between manufacturers, regulators and healthcare authorities Exchange of post-market vigilance information Supporting inventory control in hospitals Purchasing and supply chain management The GMDN is recommended by the International Medical Device Regulators Forum IMDRF and is now used by over 70 national medical device regulators to support their activity.
The GMDN gmdn code list not yet specified for the UDI database system proposed in new European Regulations [5] intended to be used by manufacturers of medical devices who have their own UDIs unique device identifiers and traceability.
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