Taiwan FDA registration d212738fec30a49baa38d693715694da
"Youkang" fiber optic ureteral nephroscopy
TW: “佑康”光纖輸尿管腎鏡
Taiwan·Risk Class 2·YouCare Technology Co., Ltd. (Wuhan)·Registered Oct 19, 2022 – Oct 19, 2027ActiveRegistration details
- Analysis ID
- d212738fec30a49baa38d693715694da
- Customs Code
- DHA09200141504
Company information
- Manufacturer
- YouCare Technology Co., Ltd. (Wuhan)
- 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
- Chinese goods;; input
Dates and status
- Registration Date
- Oct 19, 2022
- Expiry Date
- Oct 19, 2027
About this record
Access comprehensive regulatory information for "Youkang" fiber optic ureteral nephroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d212738fec30a49baa38d693715694da and manufactured by YouCare Technology Co., Ltd. (Wuhan). The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.
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