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The face-to-face meetings are really important and safe us a lot of time.“, ‘We found the collaboration with the CE Team very helpful, professional, fast and flexible. RCA R43F6FHD-EU - EC Declaration of Conformity GB/DE. must have a Declaration of Conformity. There are many bodies that enforce CE marking legislation to prevent misuse of the CE marking and to ensure that product safety is maintained to a high standard. Each directive covering your product specifies whether an authorised third party (Notified Body) must be involved in the conformity assessment procedure necessary for CE marking. This is because the DoC is the official document that states that a product meets all EU health and safety requirements and can therefore legally bear the CE mark. “CE is our partner for over 10 years and the relationship is outstanding. 2014/35/EU 2014/30/EU 2009/125/EC EC/1275/2008 2011/65/EU And are produced under a quality scheme at least in conformity with ISO 9001 or CENELEC Permanent Documents Only for Medical Devices produced under a quality scheme at least in conformity with EN13485: The Notified Body: performed: (Name and number) and issued the certificate: EC declaration of conformity. If you need help identifying whether a Declaration of Conformity is valid you can contact us. The Declaration of Conformity document needs to include the following: Name/address of manufacturer (and of responsible person where applicable) Model and/or serial number of equipment However, the formal name for the document is the Declaration of Conformity. Luckily, you only need to comply with 2 main ones and some measures specific to your products (see table below). This is not obligatory for all products, so it is important to check whether the involvement of a Notified Body is required. The manufacturer or Authorised Representative must keep the Declaration of Conformity on file for ten years from the date that the product is placed on the market (unless otherwise mentioned in the applicable Directives). Directive of the European Parliament and of theCouncil of 26 February 2014 on the harmonisation of the laws By drawing up and signing the EU Declaration of Conformity, the manufacturer assumes responsibility for the compliance of the product. It is a mandatory document prescribed by most of the European directives and regulations. EU TOY DIRECTIVE: EC DECLARATION OF CONFORMITY (DoC) A REQUIREMENT FOR MANUFACTURERS It is a new requirement set by the Toy Safety Directive2009/48/EC. to which this declaration relates, is in conformity with the requirements of the following EC Directives: • Council Directive 2006/95/EC on the harmonization of the laws of the Member States relating to electronic equipment designed for use within certain voltage limits. However, the formal name for the document is the Declaration of Conformity. If you need help identifying whether a Declaration of Conformity is valid you can contact us. What is an EU/EC Declaration of Conformity? OCX . Do you have more questions about the EU/EC Declaration of Conformity? They are both related to the EU Declaration of Conformity (EU DoC). Before writing the Declaration of Conformity, you must have carried out these steps: As a manufacturer, it is your responsibility to draw up a Declaration of Conformity and to ensure that it includes all of the necessary information. Before writing the Declaration of Conformity, you must have carried out these steps: Identify the EU requirements for your product, Check whether your product meets the specific requirements, Check whether your product must be tested by a, It is the responsibility of the manufacturer or. In the document the manufacturer, or … EU declaration of conformity. The contact information of the manufacturer/AR is indicated on the DoC. It: By placing the CE marking on a product a manufacturer is declaring, on his sole responsibility, conformity with all of the legal requirements to achieve CE marking. Object of the declaration: Listed above. Are you importing, distributing, or manufacturing products intended for use in the EU? We, Rosemount Inc. 8200 Market Boulevard . After reviewing our documentation, they gave us structured feedback and showed us a way forward to compliance with EU directives.’, “Our partnership with Certification Expert helps to bring high added value to our Industrial AI & IoT computer platforms, furthermore their services contribute to purse our objective of making AI&IIoT solutions easier to adopt for our customers.”, “Certification Experts has a great service with high flexibility and really quick response time. We experienced this as a pleasant and valuable result. All supporting documentation are retained under the promises of the manufacturer. All products require an EU/EC Declaration of Conformity in order to be sold in the European Union. We can help you verify that the DoC meets and mentions all relevant standards and necessary testing procedures to ensure that it meets the legal requirements of the applicable Directive(s). This is an official variation of the declaration of conformity. The manufacturer is thus ensuring validity for that product to be sold throughout the EEA. It is always good to have a partner at hand who can help with profound expertise whenever required. Harmonised European standards are issued with reference to the applied directives and express the essential safety requirements in detailed technical terms. By drawing up and signing the CE Declaration of Conformity, the manufacturer becomes responsible for the product’s conformity. If you manufacture a product you need to establish the technical documentation required by the directive(s) for the assessment of the product’s conformity to the relevant requirements, and for the risk assessment. The EU Declaration of Conformity (DoC) is the manufacturer’s declaration that the product complies with those directives. Before you place a CE marking on a product, you need to establish which EU New Approach Directives apply to your product. Our experts can help you draft a Declaration of Conformity and determine whether a product’s DoC mentions all relevant standards and testing procedures. The EU directive(s) relevant to your product will mention all of the information that your Declaration of Conformity needs to include. You can read the CE marking regulations on the Europa website. EUROPEAN DECLARATION OF CONFORMITY (Prohlášení o shodě v EU) We, PHILIPS CONSUMER LIFESTYLE B.V. (Company name / Jméno) Philips Consumer Lifestyle B.V. TUSSENDIEPEN 4, 9206 AD DRACHTEN, THE NETHERLANDS (address / adresa) declare under our responsibility that the product(s) (Prohlašujeme na svou odpovědnost, že elektrický výrobek) Philips Our experts can help you draft a Declaration of Conformity and determine whether a product’s DoC mentions all relevant standards and testing procedures. The manufacturer or Authorised Representative must keep the Declaration of Conformity on file for ten years from the date that the product is placed on the market (unless otherwise mentioned in the applicable Directives). HKC NK40F1FHD-EU - EC Declaration of Conformity GB/FR. EC / EU – declaration of conformity HERFORDER ELEKTROMOTOREN-WERKE GmbH & Co. KG D – 32051 Herford Goebenstraße 106 Tel. EU DECLARATION OF CONFORMITY We, of Shure ... following applicable European Directives and their associated norms: Directive Applicable Standards General Product Safety Directive 2001/95/EC By the inherent nature of its design, this product does not present a safety risk to the user. Any modifications on the product manufactured specifications lay out this declaration. All content is available under the Open Government Licence v3.0, except where otherwise stated, Department for Business, Energy & Industrial Strategy, Check if you need to use a different conformity marking, The manufacturer’s Declaration of Conformity, placing manufactured goods on the market in Great Britain, placing manufactured goods on the market in Northern Ireland from Great Britain, placing manufactured goods on the market in Northern Ireland from the, Placing manufactured goods on the market in Great Britain, Placing manufactured goods on the market in Northern Ireland, Coronavirus (COVID-19): guidance and support, Transparency and freedom of information releases, shows that the manufacturer has checked that these products meet, is an indicator of a product’s compliance with, allows the free movement of products within the European market, cableway installations designed to carry persons, equipment and protective systems intended for use in potentially explosive atmospheres, radio and telecommunications terminal equipment, you must not place any marking or sign that may misconstrue the meaning or form of the, other markings placed on the product must not cover up the, if you reduce or enlarge the size of your marking the letters, how the product conforms to the relevant national standards, addresses of manufacture and storage places, which New Approach Directives apply to the product and how they have been met, European Community type-examination certificates, if applicable, indicate that the product meets all the necessary requirements of the directives applicable to the specific product, make sure it has the name and address of the manufacturer together with information about the product, for example brand and serial number, the Medicines and Healthcare products Regulatory Agency. 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