weinisi°ÄÃÅ¡¤ÍþÄá˹ÈË(Öйú)¹Ù·½ÍøÕ¾



ÐÂÎÅ
µ±Ç°Î»Ö㺠Ê× Ò³ >> ÐÂÎÅÖÐÐÄ >>ÐÐÒµÐÂÎÅ

Ò½ÁÆÆ÷е½ø¿Ú´úÀíÁ÷³Ì Ò½ÁÆÆ÷е½ø³ö¿ÚÁ÷³Ì

µã»÷´ÎÊý£º ´Î
·¢²¼ÈÕÆÚ£º 2016-01-21 09:40:03
À´Ô´£ººÓÄÏÍþÄá˹ҽÁƵç×ӹɷÝÓÐÏÞ¹«Ë¾
·ÖÏí

Ò»¡¢Ò½ÁÆÆ÷е½ø¿ÚÐèÒª¾ß±¸µÄ×ÊÖÊ£º £¨Ò»£©½ø¿ÚÒ½ÁÆÆ÷еµ¥Î»Ó¦¾ß±¸µÄ×ÊÖÊ

¡¡¡¡1¡¢Ò½ÁÆÆ÷е¾­ÓªÐí¿ÉÖ¤£»

¡¡¡¡2¡¢ÓªÒµÖ´ÕÕ¡¾¾­Óª·¶Î§ÀïÓÐÏúÊÛÒ½ÁÆÆ÷еÐí¿É¡¿£»

¡¡¡¡3¡¢½ø³ö¿ÚȨ¡¾ÈôûÓпÉÒÔÕÒÓнø¿ÚÒ½ÁÆÆ÷е×ÊÖʵĽø³ö¿Ú¹«Ë¾´úÀí½ø¿Ú¡¿

¡¡¡¡£¨¶þ£©½ø¿ÚÒ½ÁÆÆ÷еʱÐèÒªÌṩµÄÎļþ£º

¡¡¡¡1¡¢¹ú¼ÒʳƷҩƷ¼à¶½¹ÜÀí¾Ö°ä·¢µÄ½ø¿ÚÒ½ÁÆÆ÷еע²áÖ¤ÓëÒ½ÁÆÆ÷еע²áµÇ¼Ç±í£»

¡¡¡¡2¡¢ÊôÓÚ¡¶ÊµÊ©Ç¿ÖÆÐÔ²úÆ·ÈÏÖ¤µÄ²úƷĿ¼¡·ÄÚµÄÒ½ÁÆÆ÷е£¬Ó¦µ±ÌṩÖйúÇ¿ÖÆÐÔÈÏÖ¤Ö¤Ê飨3C£©£»

¡¡¡¡3¡¢²¿·ÖÉ豸ÐèÒª°ìÀí×Ô¶¯½ø¿ÚÐí¿ÉÖ¤¡¾OÖ¤¡¿£»

¡¡¡¡4¡¢É豸µÄÕÕÆ¬¡¢ÃúÅÆ¡¢É豸¼¼Êõ²ÎÊý¡¢×îÖÕÓÃ;¡¢ÖÐÎÄ˵Ã÷ÊéµÈ£»

¡¡¡¡5¡¢½ø¿ÚºÏͬ¡¢Ïäµ¥¡¢·¢Æ±£»

¡¡¡¡6¡¢ÆäËûÐèÒª²¹³äµÄ²ÄÁÏ¡£

¡¡¡¡¶þ¡¢Ò½ÁÆÆ÷е½ø¿ÚÇ幨Á÷³Ì£º

¡¡¡¡1¡¢¹úÍ⹩ӦÉÌ·¢»õ£»

¡¡¡¡2¡¢º£ÔËÖÁ¹úÄÚÂëÍ·»ò¿ÕÔËÖÁ»ú³¡£»µ½¸Ûºó´¬¹«Ë¾£¨º½¿Õ¹«Ë¾£©¼Äµ½»õ֪ͨÊ飻

¡¡¡¡3¡¢Æ¾µ½»õ֪ͨÊéÓëÌáµ¥µ½´¬¹«Ë¾»»µ¥£»

¡¡¡¡4¡¢¸ù¾Ý²úÆ·µÄ¼à¹ÜÌõ¼þ£¬ÒÀÉ̼ì¾ÖÒªÇó°ìÀíÏàÓ¦¼ìÑé¼ìÒßÊÖÐø£»

¡¡¡¡5¡¢±¨¹Ø£¨Æ¾Ìáµ¥¡¢Èë¾³»õÎïͨ¹Øµ¥£¬±¨¹ØÉêÇëµ¥µÈ»ò²úÆ·¼à¹ÜÒªÇóËùÐèÆäËûÎļþ£©

¡¡¡¡6¡¢º£¹ØÊÜÀí£»º£¹ØÉó¼Û£¨½ÓÊÜÉ걨¼Û¸ñͨ¹ý»òº£¹ØÖ¸¶¨»õÖµ»òº£¹ØÏµÍ³²éѯ¼Û¸ñ´èÉ̵ȣ©£»

¡¡¡¡7¡¢³ö˰µ¥£¨¹ØË°Ë°Æ±¡¢Ôöֵ˰Ʊ£©£¬½ÉÄÉ˰¿î£»

¡¡¡¡8¡¢ÂëÍ·Ìá¹ñ£»

¡¡¡¡9¡¢Ë³Àûͨ¹Ø¡¢·ÅÐС¢ÔËÊäÖÁÖ¸¶¨µØµã¡£

¡¡¡¡Èý¡¢½ø¿ÚÒ½ÁÆÆ÷еע²áÖ¤°ìÀíËùÐè×ÊÁÏ£¨ÓÐЧÆÚËÄÄ꣬ÓÐЧÆÚÂúǰ6¸öÔÂÓ¦ÉêÇëÖØÐÂ×¢²á£©

¡¡¡¡1¡¢¾³ÍâÒ½ÁÆÆ÷еע²áÉêÇë±í

¡¡¡¡Application form for registration of import medical device

¡¡¡¡2¡¢Ò½ÁÆÆ÷еÉú²úÆóÒµ×ʸñÖ¤Ã÷

¡¡¡¡Legal Qualification certification for medical device manufacturing enterprise.

¡¡¡¡3¡¢É걨ÕßµÄÓªÒµÖ´ÕÕ¸±±¾ºÍÉú²úÆóÒµÊÚÓèµÄ´úÀí×¢²áµÄίÍÐÊé

¡¡¡¡A Copy of applicant¡¯s business license and proxy for registration entrusted by the Manufacturing enterprise

¡¡¡¡4¡¢¾³ÍâÕþ¸®Ò½ÁÆÆ÷еÖ÷¹Ü²¿ÃÅÅú×¼»òÈϿɵĸòúÆ·×÷ΪҽÁÆÆ÷е½øÈë¸Ã¹ú£¨µØÇø£©Êг¡µÄÖ¤Ã÷Îļþ

¡¡¡¡Documents proving that the product can enter a certain country (or region) as medical

¡¡¡¡Device approved or accepted by the medical device competent departments of overseas governments

¡¡¡¡5¡¢ÊÊÓõIJúÆ·±ê×¼£¨¼°ËµÃ÷£©

¡¡¡¡Applicable product standard and instructions

¡¡¡¡6¡¢Ò½ÁÆÆ÷е˵Ã÷Êé

¡¡¡¡Specification for medical device

¡¡¡¡7¡¢Ò½ÁÆÆ÷е¼ì²â»ú¹¹³ö¾ßµÄ²úÆ·×¢²á¼ì²â±¨¸æ£¨ÊÊÓÃÓÚµÚ¶þÀà¡¢µÚÈýÀàÒ½ÁÆÆ÷е£©

¡¡¡¡Test report on product registration given by medical device inspection institutions(applicable to Class II and Class III medical device)

¡¡¡¡8¡¢Ò½ÁÆÆ÷еÁÙ´²ÊÔÑé×ÊÁÏ

¡¡¡¡Medical device clinical trials report.

¡¡¡¡9¡¢Éú²úÆóÒµ³ö¾ßµÄ²úÆ·ÖÊÁ¿±£Ö¤Êé

¡¡¡¡Product Quality Guarantee issued by the manufacturer certifying that the quality of the product to be registered for sale in China is exactly the same as that of the product marketed in the country (region) of origin.

¡¡¡¡10¡¢Éú²úÆóÒµÔÚÖйúÖ¸¶¨´úÀíÈ˵ÄίÍÐÊé¡¢´úÀíÈ˵ijРŵÊé¼°ÓªÒµÖ´ÕÕ»òÕß»ú¹¹µÇ¼ÇÖ¤Ã÷

¡¡¡¡Proxy of assigned agent of the manufacturer enterprise in china, written Commitment of the agent and business license or registration certificate of the agent

¡¡¡¡11¡¢ÔÚÖйúÖ¸¶¨ÊÛºó·þÎñ»ú¹¹µÄίÍÐÊé¡¢±»Î¯Íлú¹¹µÄ³Ð ŵÊé¼°×ʸñÖ¤Ã÷Îļþ

¡¡¡¡Letter of Authorization for designated after-sales service agency in China and Letter of Promisa and business license of the authorized agency.

¡¡¡¡ËÄ¡¢½ø¿ÚÒ½ÁÆÆ÷еÃâ˰Ìõ¼þ¼°°ìÀí³ÌÐò

¡¡¡¡1¡¢Ò½ÁÆÆ÷е½ø¿ÚÃâ˰Ìõ¼þ

¡¡¡¡·ÇÓªÀûÐÔÒ½ÁÆ¡¢¿ÆÑС¢½Ìѧµ¥Î»ÓÃÓÚÉíÌåµÄ¿µ¸´¡¢¿ÆÑС¢½ÌѧµÄ½ø¿ÚÒÇÆ÷É豸£¬·ûºÏÃâ˰Ìõ¼þµÄ¿ÉÃâÕ÷½ø¿Ú¹ØË°¡£

¡¡¡¡2¡¢½ø¿ÚÒ½ÁÆÆ÷еÃâ˰ÉêÇëÁ÷³Ì

¡¡¡¡¡¾1¡¿µ½ÏîÄ¿Ö÷¹Ü²¿ÃÅÉêÁì¡¶¹ú¼Ò¹ÄÀø·¢Õ¹µÄÄÚÍâ×ÊÏîĿȷÈÏÊé¡·£¬Æ¾È·ÈÏÊéµ½º£¹Ø°ìÀí¼õÃâ˰ÊÖÐø¡£

¡¡¡¡¡¾2¡¿¼õÃâ˰ÏîÄ¿º£¹Ø±¸°¸ÉóÅúÁ÷³Ì°ìÀí£º

¡¡¡¡1¡¢ÉêÇ뵥λÌṩ¼õÃâ˰±¸°¸ËùÐèµ¥Ö¤Îļþ£»

¡¡¡¡2¡¢ÉêÇ뵥λÌîд¡¶Õ÷Ãâ˰֤Ã÷ÉêÇë±í¡·£¬²¢µ½Ô¤Â¼ÖÐÐÄԤ¼£»

¡¡¡¡3¡¢ÉêÇ뵥λ³ÖËùÐèµ¥Ö¤¼°Ô¤Â¼±íÌá½»º£¹Ø±¸°¸³õÉó£»

¡¡¡¡4¡¢º£¹Ø½øÐÐÈý¼¶ÉóÅú¡£


Ò½ÁÆÆ÷е½ø¿Ú´úÀíÁ÷³Ì Ò½ÁÆÆ÷е½ø³ö¿ÚÁ÷³Ì