|
||||||||||
|
||||||||||
|
|
Certification according to EU directive 96/98/EC as amended (MED)
Equipment fitted on new ships flying European Community Administration flags and new equipment fitted on existing ships flying European Community Administration flags, when such equipment are listed in Annex A.1 to the European Directive in force amending Directive 96/98/EC (Marine Equipment Directive - MED), are subject to the provisions foreseen in the MED.
Depending on the equipment, MED may require different certification processes based on EC type examination (Module B), single product verification (Module G), product verification (Module F), production Quality Assurance (Module D), product Quality Assurance (Module E) and their combinations as listed below:
For each product, the possible procedures for conformity assessment and for the consequent issuing of certificates by RINA are given in the tables of Annex A.1 of the applicable MED directive. Where the tables of Annex A.1 to the applicable Directive indicate alternative certification paths among those indicated in the above figure, the Manufacturer may choose the one most suitable among those allowed. In any event, once a scheme has been selected, all the equipment produced and certified is considered equivalent irrespective of the Modules used.
|
DOCUMENTSRINA Rules Certificate according to MED BROCHURE |
|
ABOUT US | PRIVACY | CERTIFICATES AND STATEMENTS P.IVA 03794120109 RINA S.p.A. - Sede legale in Via Corsica 12, Genova - Capitale sociale € 30.192.800 i.v. - Registro Imprese di Genova n. 03794120109 CREDITS |