Taiwan FDA registration 319c8ed4919c77087be7e0248c49dc5e
"Fu Sheng" single-use electronic bladder renal pelvis endoscope
TW: “甫笙”一次性使用電子膀胱腎盂內視鏡
Taiwan·Risk Class 2·ZHUHAI PUSEN MEDICAL TECHNOLOGY CO., LTD·Registered Jul 19, 2023 – Jul 19, 2028ActiveRegistration details
- Analysis ID
- 319c8ed4919c77087be7e0248c49dc5e
- Customs Code
- DHA09200148308
Company information
- Manufacturer
- ZHUHAI PUSEN MEDICAL TECHNOLOGY CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- CANASONIC CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 19, 2023
- Expiry Date
- Jul 19, 2028
About this record
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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