Nursing Course Subject List

However, if doctor device intended medical administer a medicinal product andthe medicinal product are put on doctor market in such a way that they form asingle integral product which is intended exclusively for use in doctor givencombination and which is not reusable, that single integral product shall begoverned by Directive 2001/83/EC orRegulation EC No 726/2004, as suitable. In that case, therelevant time-honored safety and functionality necessities set out in Annex I tothis Regulation shall apply as far as doctor safety and performance of doctor devicepart of doctor single integral product are concerned. 10. Any device which, when put on doctor market or putinto provider, carries, as a vital part, non viable tissues or cells ofhuman origin or their derivatives which have an action ancillary medical that of thedevice shall be assessed and accredited according to medical help Regulation. Inthat case, doctor provisions for donation, procurement and checking out laid down inDirective 2004/23/EC shall apply. However, if doctor action of those tissues or cells or their derivatives isprincipal and never ancillary medical that of doctor device and doctor product is notgoverned by Regulation EC No 1394/2007, doctor product shall begoverned by Directive 2004/23/EC.