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Antigo 03-06-2010, 12:48   #11
Carlsbergman
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Boas...
Possuo um m3 dos novos com filtro particulas. A questão é que nunca senti nenhuma regeneração no filtro de particulas do carro! A luz nunca acendeu, e eu ate faço alguma cidade! Já alguem tpresenciou a regeneração do filtro de particulas? será que estes filtros não regeneram? o carro tem agora 16.000 km's!
Abraços

eu sou muito ignorante. alguém me pode explicar qual a função desta coisa e em que consiste a sua regeneração?
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Antigo 04-06-2010, 00:31   #12
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boas pessoal tenho uma duvida
tenho um m3 mas nestes dias parei num stop e foi-se abaixo e depois nao queria pegar depois tentei colocalo no passeio pra nao interronper o transito e com a marcha-a- traz e a dar a chave pegou e depois nao falhou nem acendeu luzes nenhumas e agora ja nao pega outravez e leveio a uma oficina e o mecanico diz-me que nao chega gasoleo ao motor alguem tem uma ideia do que possa ser ??????
talvez filtro entupido ou a bomba que puxa o gasoleo pode nao estar a puxar.
alguem mais entendido no assunto ja te vem dizer alguma coisa.

Rimo chamado a recepçao!!!
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Antigo 07-06-2010, 15:29   #13
fonseca84
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talvez filtro entupido ou a bomba que puxa o gasoleo pode nao estar a puxar.
alguem mais entendido no assunto ja te vem dizer alguma coisa.

Rimo chamado a recepçao!!!


obrigado
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Antigo 18-06-2010, 10:03   #14
fonseca84
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ja tenho o m3 reparado foi a bomba do gasoleo que desferou mas nimguem precebe pk nem os mecanicos da mazda porque ele tinha gasoleo e disserao que podera vir a acontecer de novo ou nao enfim a coisas esquesitas
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Antigo 24-09-2021, 13:49   #15
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Antigo 13-10-2021, 17:04   #16
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Predefinido ISO Standardization Is Essential To The Growth Of Businesses

Part 1: Safety And Performance Requirements For Medical Electrical Equipment. Collateral Standard: Usability En 60601-1-6:2010
Innovative technologies are accelerating the advancement of medical equipment and electrical devices. The product is becoming sought-after as the scale of production increases. EN 60601-1-1:1-6:2010 describes the procedure that a manufacturer employs to evaluate the product's specifications, design the necessary documentation, verify and confirm usability. This is applicable to medical equipment's fundamental safety and performance. The usability engineering process analyzes and minimizes risks from issues with usability that are associated with the proper use. This is an important standard to be aware of if your company involves the manufacture of medical equipment. See the most popular cen catalog tc cen-tc-248-wg-17 site.

Innovation Management - Foundations And The Vocabulary (Iso 56000,2020) EN ISO 56000:2021
Explanatory documents are created for technical standards, for instance, providing the security of information. This is in order to avoid confusion about the meaning of the word. EN ISO 56000: 2021 is a great example. This document outlines the fundamental concepts and vocabulary for innovation management as well as its methodical implementation. It is applicable to:A) Companies that have an innovation management system or conduct assessments of innovation management.B) Organizations that need to improve the effectiveness of their innovation management processesc. Customers, users and other relevant parties (e.g. Partners, suppliers, funders university, investors or public authorities, etc.) who seek to have faith in the capabilities of innovation and efficiency of an organization.D. Organizations and other parties who want to enhance communication through a common understanding about the vocabulary used for innovation managemente. Training providers in assessment, training, or consulting for innovation management , system innovation management;f) The developers of innovation management and related standard1.2 This document is meant to be applicable to:b) All types of innovation, e.g. Any type of innovation which include service, product and model. They could be either radical or incremental.C) All kinds of approaches, e.g. External and internal innovation, in addition to market-, technology and design-driven innovations.This document defines all applicable terms and definitions of the ISO/TC 279 standard on innovation management.The standard is packed with crucial clarifications. We recommend that your take the time to read them and check their accuracy with your technological base to make certain that they are the most appropriate document to utilize to promote your business at an international level. Check out the top iso catalog standards iso-24627-3-2021 info.

The Characterisation Of Bulk Materials: Determination Of A Size-Weighted Fine Fraction And The Content Of Crystalline Silica - Part 1 General Information And Selection Of Testing Methods EN 17289-1:2020
Regulators are complex locally as well as globally due to the vast variety of materials used in production. International standards are currently being developed to facilitate the entry of companies and organizations to new markets.This document provides information on the testing requirements and methods that can be used to determine the dimensions of the fine portion of crystal silica (SWFFCS), in bulk materials.This document gives also guidance regarding the preparation of the sample and determination of crystallized silica through the X-ray powder diffractometry (XRD) as well as Fourier Transform Infrared Spectroscopy (FT-IR).EN 17289-2 describes how to determine the size-weighted percentage of fine particles using the size distribution that is measured. It is based on the assumption that the size distribution of the crystal quartz particles are the exact same as that of other particles found in the bulk material. EN 1789-3 describes the procedure for liquid sedimentation to calculate the size weighted fine fraction of crystal silica. Both methods have limits and assumptions. These limitations are outlined in EN 1728-9, EN 17289-3. If validated properly and validated, the EN 17289-3 method can also be applied to other constituents.This document is applicable to crystalline silica containing bulk materials that have been thoroughly researched and validated for the determination of the size weighted fine fraction or the crystalline silica.If your area of work is in contact with the material specified in the description of this document, then its presence in the technological documentation base of your company will greatly assist in expanding production. Our website provides more detail. See the best clc catalog standards en-60603-4-1998 site.

Methodology For Reducing The Environmental Impact Of Product Design And Development For Mechanical Devices EN 16524:2020
As new technology is developed and air pollution becomes more reported the environmental and safety issues continue to evolve. One of the documents that offer solutions to this issue is EN 16524: 2020.This document outlines a method to reduce the environmental impact of design for products. It's tailored to mechanical products.This approach is well-suited for revising an existing product. If assumptions regarding a virtual reference product are established, the technique can be applied to design an entirely new product. This methodology is intended to be used by companies that are adopting an ecodesign strategy to maximize the environmental impact of products throughout their lifecycles.It also meets certain requirements of ISO 14001 2015 regarding the integration environmental aspects in product design. This document is intended for people directly involved in designing and making mechanical products as in addition to decision makers and managers that must define corporate policies. The methodology proposed is designed to help kickstart ecodesign initiatives within businesses in a teaching and continuous improvement process.This document includes a template for companies to use in their communication regarding the environment. This document cannot be used to compare products (even those of similar suppliers). The document isn't appropriate for product certification.This is a crucial document in the 21st century. That's why you should research the possibility of getting it and how to incorporate it into your business activities. See the most popular cen catalog standards cen-clc-tr-14060-2014 info.

Health Informatics Interoperability Of Devices Part 20701: Point-Of-Care Medical Device Communication - Service-Oriented Medical Device Exchange Architecture And Protocol Binding (Iso/Ieee 11073-20701:2020) EN ISO 11073-20701:2020
Communication technologies are not only used in areas that are closely related to this group however, they are also employed in the medical field. In order to facilitate the use of medical devices, it is difficult and requires the reorganization of the existing technology. International documents have been developed, including EN ISO 11073-20701 2020.
This standard defines a service-oriented device architecture for medical devices, and protocols for communication in medical IT systems. These systems for medical IT require the ability to secure and safely manage PoC medical devices. It defines the functional components as well as their connections to each other.This document is highly specific and has a low profile. Therefore, we suggest that you go through the technical specifications and speak with managers who specialize in international document choices for any additional questions. See the most popular sist catalog standards sist-en-1397-2015-ac-2016 site.

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