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- Notified_Body abstract "A Notified Body, in the European Union, is an organization that has been accredited by a Member State to assess whether a product meets certain preordained standards. Assessment can include inspection and examination of a product, its design and manufacture. For example, a Notified Body may designate that a medical device conforms to the EU Medical Devices Directive, which defines the standards for medical devices. With this Declaration of Conformity, the manufacturer can label the product with the CE Mark, which is required for distribution and sale in the EU.EU member states will then inform the European Commission whether a product complies with set standards or not, and the names of bodies will be disclosed.More generally, a Notified Body is a third-party, accredited body which is entitled by an Accreditation Body. Upon definition of standards and regulations, the Accreditation Body may allow a Notified Body to provide verification and certification services. These services are meant to ensure and assess compliance to the previously defined standards and regulations, but also to provide an official certification mark or a declaration of conformity.For instance, TÜV Rheinland is an officially recognized Notified Body for the Pressure Equipment Directive PED 97/23/EC and can therefore provide pressure vessel certification, inspection and testing services to guarantee product compliance to the defined safety regulations.".
- Notified_Body thumbnail Conformité_Européenne_(logo).svg?width=300.
- Notified_Body wikiPageExternalLink index.cfm?fuseaction=directive.main.
- Notified_Body wikiPageExternalLink papers.cfm?abstract_id=1674209.
- Notified_Body wikiPageID "19999597".
- Notified_Body wikiPageRevisionID "602297550".
- Notified_Body hasPhotoCollection Notified_Body.
- Notified_Body subject Category:Product_certification.
- Notified_Body comment "A Notified Body, in the European Union, is an organization that has been accredited by a Member State to assess whether a product meets certain preordained standards. Assessment can include inspection and examination of a product, its design and manufacture. For example, a Notified Body may designate that a medical device conforms to the EU Medical Devices Directive, which defines the standards for medical devices.".
- Notified_Body label "Aangemelde instantie".
- Notified_Body label "Benannte Stelle".
- Notified_Body label "Notified Body".
- Notified_Body label "Organisme notifié".
- Notified_Body label "Organismo notificato".
- Notified_Body sameAs Notifikovaná_osoba.
- Notified_Body sameAs Benannte_Stelle.
- Notified_Body sameAs Organisme_notifié.
- Notified_Body sameAs Organismo_notificato.
- Notified_Body sameAs Aangemelde_instantie.
- Notified_Body sameAs m.04yh1gh.
- Notified_Body sameAs Q816676.
- Notified_Body sameAs Q816676.
- Notified_Body wasDerivedFrom Notified_Body?oldid=602297550.
- Notified_Body depiction Conformité_Européenne_(logo).svg.
- Notified_Body isPrimaryTopicOf Notified_Body.