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This document certifies that the paint system consisting of Mammut Primer and Pilot II complies with the relevant marine equipment regulations and standards.
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How to fill out ec type-examination certificate

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How to fill out EC TYPE-EXAMINATION CERTIFICATE

01
Gather necessary documents: Ensure you have all relevant technical documentation of the product.
02
Identify the type of product: Clearly define the product classification according to EC directives.
03
Complete the application form: Fill out the designated application form for EC type-examination, providing accurate details about the product.
04
Provide supporting documents: Include any required certificates, drawings, specifications, and test reports.
05
Submit the application: Send your completed application and supporting documents to a notified body.
06
Await assessment: Allow the notified body to review your application and perform necessary testing.
07
Receive the certificate: If compliant, you will receive the EC type-examination certificate, which formally recognizes that your product meets EU standards.

Who needs EC TYPE-EXAMINATION CERTIFICATE?

01
Manufacturers wishing to sell products in the EU that require compliance with specific directives.
02
Companies producing equipment or machinery that must meet health and safety standards.
03
Importers bringing non-EU products into the EU market that must undergo compliance testing.
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People Also Ask about

Type examination is the part of a conformity assessment procedure in which a Notified Body examines the technical design of PPE and verifies and attests that the technical design of the PPE meets the requirements of the Regulation that apply to it.
Means the procedure whereby an authority of an EU Member State certifies that a type of vehicle, system, component or separate technical unit satisfies relevant technical requirements and administrative provisions listed in the relative instrument.
The certificate is only part of the CE-marking process We can say that the procedure for passing the audit by the notified body and obtaining the EC-certificate is the final check of what the manufacturer has done before in order to achieve compliance with European regulatory requirements.
Design Examination Certificate means certification that the examination of a medical device by a Notified Body has proven that the design of such medical device meets the requirements of the applicable European Council Directives, such as European Council Directive 93/42/EEC.
The EC Certificate authorizes the manufacturer to affix the CE marking to their device, enabling its legal placement on the EU market. The certificate demonstrates that: The device conforms to the applicable safety and performance standards.
Means the procedure whereby an authority of an EU Member State certifies that a type of vehicle, system, component or separate technical unit satisfies relevant technical requirements and administrative provisions listed in the relative instrument.
ec·​type. ˈekˌtīp. 1. : a copy from an original : an imitation or reproduction (such as an impression of a seal)

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The EC Type-Examination Certificate is an official document issued by a notified body that certifies that a particular product or equipment meets the essential requirements set out in relevant European directives.
Manufacturers or their authorized representatives are required to file the EC Type-Examination Certificate when they seek to prove compliance of their products with European standards and regulations.
To fill out the EC Type-Examination Certificate, manufacturers must provide detailed information about the product, including specifications, design, and testing results, ensuring that all required fields are accurately completed according to the templates provided by the notified body.
The purpose of the EC Type-Examination Certificate is to demonstrate that a product complies with the relevant safety and performance requirements of European legislation, allowing it to be marketed in the European Economic Area.
The EC Type-Examination Certificate must report information such as the manufacturer's name and address, product identification, the applicable regulations and standards, results of assessments, and details about the notified body that conducted the assessment.
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