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This document declares the compliance of the FFP2 masks with European standards and directives, ensuring their ergonomics, comfort, and safety features.
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How to fill out EC declaration of conformity

01
Identify the relevant EU legislation applicable to your product.
02
Ensure that your product complies with the essential requirements outlined in the applicable legislation.
03
Perform necessary conformity assessments, including testing and inspections, to verify compliance.
04
Compile technical documentation that includes design and manufacturing details, risk assessment, and test results.
05
Draft the EC declaration of conformity using the correct format, including product identification, manufacturer's information, and applicable regulations.
06
Sign and date the declaration, and ensure it is readily available to authorities and customers.

Who needs EC declaration of conformity?

01
Manufacturers of products that fall under EU legislation governing safety, health, and environmental protection.
02
Importers bringing non-EU products into the EU market.
03
Distributors who market products requiring compliance within the EU.
04
Any businesses that produce or sell products regulated by specific EU directives.
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People Also Ask about

A CE Certificate of Conformity is a third-party-issued document stating that a certain product is compliant with one or more directives, regulations, and harmonized standards.
At the end of the CE marking process the manufacturer confirms the CE marking compliance of the product by drawing up a EU Declaration of Conformity (or 'Declaration of Conformity' or 'DoC') and affixing the CE marking. The EU Declaration of Conformity previously was called an 'EC Declaration of Conformity'.
The government has laid legislation to continue recognition of current EU requirements for a range of product regulations, including the CE marking (Conformité Européene, or European Conformity marking) for a range of product regulations.
Conformité Européenne (CE) certification is a regulatory standard that verifies certain products are safe for sale and use in the European Economic Area (EEA). Manufacturers place a CE marking on certified products to indicate that the product complies with European safety rules and can be traded freely within the EEA.
A Declaration of Conformity (DoC) is a document stating that a product, usually electronic, meets the standards to which it must legally adhere, such as safety regulations.
The CE mark means that the manufacturer takes responsibility for the compliance of a product with all applicable European health, safety, performance and environmental requirements. CE stands for "Conformité Européenne", the French for European conformity.
The Declaration of Conformity must be issued by the “manufacturer” or their “authorised representative”. However, this is not necessarily the person or company who actually made the product.
When a manufacturer puts the CE marking on a product it implies that it complies with all the Essential Health and safety requirements from all the directives and regulations that applies to its product. For example, for a machine, generally the Machinery directive applies, but often also: Low voltage directive.

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The EC Declaration of Conformity is a document issued by a manufacturer or their authorized representative that states that a product meets all relevant European Union directives and regulations.
Manufacturers, importers, or their authorized representatives are required to file the EC Declaration of Conformity for products that fall under EU directives.
To fill out an EC Declaration of Conformity, one must include product information, the manufacturer's details, a statement of conformity to applicable directives, and the date of issue and signature of the authorized representative.
The purpose of the EC Declaration of Conformity is to provide assurance that a product complies with European safety and environmental requirements, facilitating its market access within the EU.
The information that must be reported includes the product name and model, the manufacturer's name and address, the list of applicable directives, the conformity assessment, and the signature and date of the authorized representative.
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