- 適應症
-
- 劑型
-
- 包裝
- 詳如中文仿單核定本、詳如中文仿單核定本。詳如中文仿單核定本。註銷規格：H965100210 (10021), H965100240 (10024), H965100370 (10037), H965100290 (10029), H965100120 (10012), H965100110 (10011), H965100190 (10019), H965100330 (10033), H965100260 (10026), H965100320 (10032), H965100100 (10010), H965100360 (10036), H965100200 (10020), H965100350 (10035), H965100340 (10034), H965100310 (10031), H965100300 (10030), H965100130 (10013), H965100160 (10016), H965100280 (10028), H965100390 (10039), H965100400 (10040), H965100180 (10018), H965100250 (10025), H965100230 (10023), H965100220 (10022), H965100270 (10027), H965100140 (10014), H965100150 (10015), H965100170 (10017), H965100380 (10038), H965100410 (10041);H965S6KIMNYFBO (KIMNY FB), 965S6KIMNYMFBO (KIMNYMFN BO); H965100450 (10045), H965100490 (10049), H965100530 (10053), M003101490 (10149), M003101530 (10153)。
- 許可證字號
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衛部藥製字第009574號
- 註銷狀態
- 1
- 註銷日期
-
2006-10-02
- 註銷理由
- 855
- 有效日期
-
2005-12-15
- 發證日期
-
2000-12-15
- 許可證種類
- 09
- 中文品名
- 蓋德導引導管
- 英文品名
- GUIDER SOFTIP GUIDING CATHETER "BOSTON SCIENTIFIC"
- 藥品類別
- E000 心臟血管用裝置
- 申請商地址
- 台北巿松山區光復北路11巷35號3樓7樓
- 通關簽審文件編號
- DHA00600957402
- 資料更新時間
-