Direttiva 93 42 cee pdf files

Direttiva 9342cee del consiglio del 14 giugno 1993 concernente i. Notified body notified to european commission under number. The light chair complies with medical devices directive 9342eec altezza minima. The dental patient chair type 2009new does not cause electromagnetic or other influences at other equipments. Certificato ce dichiarazione di approvazione del sistema qualita sistema completo di garanzia qualita tecnogaz spa 43038 sala baganza pr strada cavalli 4 ita italy visto lesito delle verifiche condotte in conformita allallegato ii, con lesclusione del punto 4, della direttiva 9342 cee e s. Council directive 9342eec of 14 june 1993 concerning medical. Conforme alla direttiva 9342 cee relativa ai prodotti medicali. Classification criteria definitions for the classification. Direttiva 93 42 cee e successive modifiche ed integrazioni, allegato v, attuata in italia con dlgs.

B council directive 9342eec of 14 june 1993 concerning. Duration transient normally intended for continuous use for less than 60 minutes. Council directive 93 42 eec of 14 june 1993 concerning medical devices the council of the european communities, having regard to the treaty establishing the european economic community, and in particular article 100a thereof, having regard to the proposal from the commission 1, in cooperation with the european parliament 2. Scarica questo file direttiva 93 42 cee testo consolidato 2007. The council of the european communities, having regard to the treaty establishing the european economic community, and in particular article 100a thereof, having regard to the proposal from the commission 1, in cooperation with the european parliament 2. This approval certificate is subjected to the provisions laid down in the rules for managing the ec. Council directive 9342eec of 14 june 1993 concerning medical devices. The machinery sector is an important part of the engineering industry and is one of the industrial mainstays of the community economy. Compliance of medical devices with the new requirements according to article 2 of directive 9342eec, member. Understanding the machinery directive 2006 42ec the directive has been put in place because. Essential requirements annex i, 9342eec as compliance.

The machinery sector is an important part of the engineering industry and is one of the. Official journal no page date m1 directive 9879ec of the european parliament and of the council of 27 october 1998 l 331 1 7. European medical device directive essential requirements. Lo stato dellarte delle poltrone dentali stateoftheart. B council directive 9342eec of 14 june 1993 concerning medical devices oj l 169, 12. Rilasciato ai sensi della direttiva 9342 cee allegato ii escl. Direttiva 9342cee del consiglio, del 14 giugno 1993, concernente i dispositivi medici.

Conformity with medical device directive 9342 eec is mandatory all devices that fit the definition of a and its accessories this directive is of the regulation remains pending. The social cost of the large number of accidents caused by the use of machinery can be reduced by. Compliance of medical devices with the new requirements according to article 2 of directive 9342eec, member states shall take all necessary steps to ensure that devices may be placed on the market andor put into service only if. Direttiva dispositivi medici 9342cee certifico srl. Official journal no page date m1 directive 9879ec of the. The council of the european communities, having regard to the treaty establishing the european. Questions relating to the implementation of directive 200747 ec 1. This approval certificate is subjected to the provisions laid down in the imq regulation for the. Council directive 93 42 eec of 14 june 1993 concerning medical devices. It is not susceptible of such influences by other equipments, as it complies with electromagnetic compatibility directive 89336eec, emended by 9231eec and 93 68eec directives, and it satisfies the requirements of. Direttiva 93 42 cee del consiglio, del 14 giugno 1993, concernente i dispositivi medici gazzetta ufficiale n. Raccolta linee guida meddev dispositivi medici certifico srl. Direttiva 9342 cee, allegato il escluso il pto 4, attuata in italia con dlgs.