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EMI Certificate

How is EMI Test done?

If the device causes any electromagnetic interference

EMI do, electromagnetic interference tests, radio frequency wave operating devices, malicious broadcasts, operating frequency and output power controls.If it is determined that the device does not cause any electromagnetic interference in such an environment, The device is successful in the EMI Test.
if the device is causing any electromagnetic interference, CE certification cannot be given to the device under test as it may disrupt the operation of other devices.

Telecommunication devices that do not meet EMI Test requirements

The devices covered by the Radio Telecommunications Terminal Equipment Directive must meet the EMI Test requirements in order to obtain CE certification.In the scope of the directive, all radio and telecommunication equipment, such as mobile phones, satellite receivers, fixed and direct phones, ADSL modem and other data modems, base stations, radio and TV transmitters, must meet the EMI Test requirements. Telecommunication devices that do not meet the EMI Test requirements may disrupt other devices or disrupt their operation.Likewise, these devices can also be damaged by interference due to this electromagnetic interference.Therefore, a telecommunication device must meet the requirements of the EMI test in order to obtain a CE certificate.

EMI test is carried out by the engineers in laboratory environment by considering different conditions. Whether or not the device causes electromagnetic interference is controlled by the Radio Telecommunication Terminal Equipment Directive with different variations.If the device does not cause any interference, it is approved for the CE certificate. Since the device or products must have CE marking in order to be circulated in the European Union free market, it is mandatory to apply EMI Test to the telecommunication products.

If the device does not cause any interference

After being tested in EMI test laboratories, being careful during the report and document phase is also very important for getting CE certificate. It is therefore necessary to be careful when choosing test laboratories.

EMI Certificate

What is EMI Test?

What is EMI Test?

EMI, electromagnetic interference tests, radio frequency wave operating devices, malicious transmissions, operating frequency and output power controls. If it is determined that the device does not cause any electromagnetic interference in the environment according to these criteria, the device will be successful in the EMI Test. However, if the device is causing any electromagnetic interference, CE certification cannot be given to the device under test as it may impair the operation of other devices.

What happens as a result of the incompatibility of EMI Test conditions?

The devices under the Radio Telecommunications Terminal Equipment Directive must meet the EMI Test requirements in order to obtain CE certification. All radio and telecommunication equipment, such as mobile phones, satellite receivers, fixed and direct telephones, ADSL modem and other data modems, base stations, radio and TV transmitters, must meet the EMI Test requirements. Telecommunication devices which do not have EMI Test conditions may disrupt other devices or disrupt their operation. Likewise, these devices can also be damaged by interference due to this electromagnetic interference. Therefore, a telecommunication device must meet the requirements of the EMI test to obtain a CE certificate.

EMI Test application and certification

EMI test is carried out by the engineers in the laboratory environment in consideration of different conditions. Whether the device causes electromagnetic interference is controlled by different variations within the scope of the Radio Telecommunications Terminal Equipment Directive. If the device does not cause any interference, it may be eligible for a CE certificate and a certificate of conformity cannot be issued if an interference is detected. EMI test is mandatory for the telecommunication products, as the device or products are required to have CE marking in order to circulate in the European Union free market.

Ege Test Center and EMI

After being tested in EMI test laboratories, being careful during the report and document phase is also very important for getting CE certificate. For this reason, being careful when choosing test laboratories, Ege Test Center supports you in EMI Tests with expert teams.

Detailed information and contact

You can contact us by e-mail to marketing@egetestcenter.com for detailed information about the EMI Test and get detailed information or you can reach us by filling out the form at https://en.egetestcenter.com/apply-online/ .

Ce Certification

How to get CE certificate?

Ege Test Center and CE Certificate

With the expert engineers trained in the defense industry and international test organizations, the CE certification works of your Ege Test Center products are completed quickly and quickly.

CE Certificate is taken following the following ways:

1. Stage Research and Detection

  • First of all, product specifications are determined by determining the technical characteristics and intended use of the product.
  • The directives entered by the product within the scope of CE are determined.
  • After determining the product directives specific standards within the scope of the directive are determined.
  • Determined if the notified body is required. Some risky product groups have a mandatory certification.
  • Roadmap is examined under the directive or directives and the most appropriate road map is selected.
  • Examining the requirements of the Quality Management System; Some directives provide for a quality system in the process of CE marking

2. Stage Test and Control process

  • Testing, analysis and technical controls of the product according to the standards determined within the scope of the directives / directives and taking the necessary reports.
  • Where necessary, obtaining certificates and test reports from the Notified Body establishment in risk product groups;
  • Doing Risk Analysis;
  • Preparation of appropriate user manual;
  • Technical Documentation / Preparation of Technical File;
  • Declaration of Conformity;

3. Stage Placing CE Marking and Storing Technical File

  • CE marking is placed on the product according to the relevant directive.
  • Store the Technical File of the Product for the period specified in the product directive and, where necessary, be archived to the competent authorities / market surveillance authorities.

4. Stage Product Launch

  • At the end of the above processes, the product is entitled to carry CE marking and it is free to have free movement in our country and EU market.

In the CE certification process, our company will prepare your CE Certificate declaration by serving you in the fields of consulting, testing, reporting and technical file preparation with the laboratory facilities of EGE TEST CENTER.

For communication and detailed information

For communication and detailed information you can click This page or send mail marketing@egetestcenter.com

European CE Marking Strategy for Medical Devices

To sell medical devices in the European Union (EU), you must obtain or apply CE Marking for your product. CE Marking indicates a product’s compliance with the applicable EU regulations and enables the commercialization of your products in 32 European countries. As a legal medical device manufacturer, you are responsible for maintaining regulatory compliance and securing CE marking for your product, regardless of whether you outsource any or all components of your manufacturing operation.

How to obtain CE marking for your medical device

CE is not a quality mark, but compliance with EU Directives requires you to meet specific standards of performance, quality, safety, and efficacy for your product type. We have a detailed chart explaining the current The basic process follows these steps:

  1. Determine which EU Directive applies to your device: Medical Devices Directive (93/42/EEC), In Vitro Diagnostic Devices Directive (98/79/EC) or Active Implantable Medical Devices Directive (90/385/EEC)
  2. Determine the classification of your device.
  3. Implement a Quality Management System, if applicable to your device. Most companies use ISO 13485 to meet the requirements.
  4. Prepare a CE Marking Technical File or a Design Dossier
  5. Select and appoint a European Authorized Representative to act on your behalf within the EU if you have no physical location in Europe.
  6. Have your QMS and Technical File/Design Dossier audited by a Notified Body, unless your device is Class I, is not sterile and has no measuring function.
  7. Obtain CE Marking and ISO 13485 certificates from your Notified Body.
  8. Prepare a Declaration of Conformity (DoC), which states that your device complies with the appropriate Directive.

For Communication and Apply

For detailed information and communication, you can send an email to us or you can fill the form by clicking this Online Application link.