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  2. CE marking - Wikipedia

    en.wikipedia.org/wiki/CE_marking

    The manufacturer draws up an EU declaration of conformity or a declaration of performance (for Construction Products) and affixes the CE marking on the product. If stipulated in the directive(s) or regulation(s), an authorized third party ( Notified Body ) must be involved in the conformity assessment procedure or in setting up a production ...

  3. European Authorized Representative - Wikipedia

    en.wikipedia.org/wiki/European_Authorized...

    An authorised representative may also carry out a conformity assessment of a medical device on behalf of the manufacturer. [ 7 ] European ‘Blue Guide" [ 8 ] describes that delegation of an authorised representative should be set out in writing (as an agreement, mandate, or power of attorney) to define contents and limits of tasks.

  4. Regulation (EU) No. 305/2011 - Wikipedia

    en.wikipedia.org/wiki/Regulation_(EU)_No._305/2011

    Clarify the affixing of CE marking to construction products. Introduce the need to issue a declaration of performance as a basis for CE marking. Define clear rules for the assessment and verification of constancy of performance (AVCP) systems applicable to construction products (former Attestation of Conformity AoC).

  5. Construction Products Directive - Wikipedia

    en.wikipedia.org/wiki/Construction_Products...

    CE Marking of construction products was introduced in the CPD in 1989. CE Marking is a declaration by the manufacturer that the product meets certain public safety requirements. The public safety requirements are a set of essential characteristics that each product must satisfy and these characteristics are given in the product's harmonised ...

  6. Notified body - Wikipedia

    en.wikipedia.org/wiki/Notified_Body

    CE Mark. A notified body, in the European Union, is an organisation that has been designated by a member state to assess the conformity of certain products, before being placed on the EU market, with the applicable essential technical requirements. These essential requirements are publicised in European directives or regulations.

  7. Type approval - Wikipedia

    en.wikipedia.org/wiki/Type_approval

    The CE mark found on the back of many electronic devices does not mean that the product has obtained type approval in the European Union. The CE mark is the manufacturer's declaration that the system/assembly meets the minimum safety requirements of all the directives (laws) applicable to it, and of itself, does not signify any third party ...

  8. Certification mark - Wikipedia

    en.wikipedia.org/wiki/Certification_mark

    Canadian certification label on a bag of rockwool Counterfeit electrical cords with false UL certification marks. A certification mark on a commercial product or service is a registered mark that enables its owner ("certification body") to certify that the goods or services of a particular provider (who is not the owner of the certification mark) have particular properties, e.g., regional or ...

  9. FCC mark - Wikipedia

    en.wikipedia.org/wiki/FCC_mark

    The FCC logo or the FCC mark is a voluntary mark employed on electronic products manufactured or sold in the United States which indicates that the electromagnetic radiation from the device is below the limits specified by the Federal Communications Commission and the manufacturer has followed the requirements of the Supplier's Declaration of Conformity authorization procedures.

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