Shfuqizuar
ISO 10993-12:2007 specifies requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical device testing in biological systems in accordance with one or more parts of the ISO 10993 series. Specifically ISO 10993-12:2007 addresses:
test sample selection;
selection of representative portions from a device;
test sample preparation;
experimental controls;
selection of and requirements for reference materials;
preparation of extracts.
ISO 10993-12:2007 is not applicable to materials or devices containing live cells.
Directives related to this standards.
Direktiva 2007/47/EC e Parlamentit Europian dhe e Këshillit të 5 shtator 2007 amendon Direktivën e Këshillit 90/385/EEC mbi përafrimin e ligjeve të Shteteve Anëtare në lidhje me pajisje medicinale aktive transplatuese, Direktiva e Këshillit 93/42/EEC në lidhje me pajisjet mjekësore dhe Direktivën 98/8/EC në lidhje me vendosjen e produkteve biocide në treg
                    WITHDRAWN
                    SSH EN ISO 10993-12:2009
                    95.99
                                        Withdrawal of Standard
                    17 maj 2013
                
                WITHDRAWN
                                    SSH EN ISO  10993-12:2012