Taiwan FDA registration 1d2d09f631bba8a10299c9ee989e6ca1
"Seexin" electronic ureteral pyeloscope
TW: “視新”電子輸尿管腎盂鏡
Taiwan·Risk Class 2·Zhuhai Seesheen Medical Technology Co., Ltd.·Registered Jan 11, 2023 – Jan 11, 2028ActiveRegistration details
- Analysis ID
- 1d2d09f631bba8a10299c9ee989e6ca1
- Customs Code
- DHA09200142609
Company information
- Manufacturer
- Zhuhai Seesheen Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- Kang Cheng Medical Technology 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
- Jan 11, 2023
- Expiry Date
- Jan 11, 2028
About this record
Access comprehensive regulatory information for "Seexin" electronic ureteral pyeloscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d2d09f631bba8a10299c9ee989e6ca1 and manufactured by Zhuhai Seesheen Medical Technology Co., Ltd.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.
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