"Fu Sheng" single-use electronic bladder renal pelvis endoscope - Taiwan Registration 319c8ed4919c77087be7e0248c49dc5e
Access comprehensive regulatory information for "Fu Sheng" single-use electronic bladder renal pelvis endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 319c8ed4919c77087be7e0248c49dc5e and manufactured by ZHUHAI PUSEN MEDICAL TECHNOLOGY CO., LTD. The authorized representative in Taiwan is CANASONIC CO., LTD..
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319c8ed4919c77087be7e0248c49dc5e
Registration Details
Taiwan FDA Registration: 319c8ed4919c77087be7e0248c49dc5e
Device Details
"Fu Sheng" single-use electronic bladder renal pelvis endoscope
TW: โ็ซ็ฌโไธๆฌกๆงไฝฟ็จ้ปๅญ่่ฑ่
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Risk Class 2

