00955     2200205   4500001002100000005001500021035002000036007000300056008004100059020001800100082001100118084001700129100003600146245022600182260006300408300000800471700002400479520013700503600010900640INLIS00000000000129020230915034103  a0010-0923000028ta230915                           0        a9786233010250  a610.28  a610.28 ANI g0 aAnita Nur Fitriana, S.Farm, Apt1 aGUIDELINES FOR EVALUATION OF MEDICAL DEVVICES AND IN VITRO DIAGNOSTIC MEDICAL DEVICES ACCORDING TO THE REGULATION OF THE MINISTER OF HEALTH OF THE REPUBLIC OF INDONESIA NUMBER 62 OF 2017 /cAnita Nur Fitriana, S.Farm, Apt  aJakarta :bKementerian Kesehatan Republik Indonesia,c2020  a2150 aTri Kaloko,Apt, dkk  aBuku pedoman ini dapat memberikan kemanfaatan yang besar bagi Tim Penilai dalam melakukan bimbingan teknis perizinan alat kesehatan. 4a1. Equipment and Supplies 2. Elektronics, Medical 3. Government Regulation 4. Medical Device Legislation