Taiwan FDA registration bf2f48247a58d2bab3b2c216c01a7188
"Weili" single-use minimally invasive dilation drainage kit
TW: “維力”一次性使用微創擴張引流套件
Taiwan·Risk Class 2·WELL LEAD MEDICAL CO., LTD.·Registered Jul 19, 2018 – Jul 19, 2028ActiveRegistration details
- Analysis ID
- bf2f48247a58d2bab3b2c216c01a7188
- Customs Code
- DHA09200094209
Company information
- Manufacturer
- WELL LEAD MEDICAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Kang Cheng Medical Technology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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, 2018
- Expiry Date
- Jul 19, 2028
About this record
Access comprehensive regulatory information for "Weili" single-use minimally invasive dilation drainage kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf2f48247a58d2bab3b2c216c01a7188 and manufactured by WELL LEAD MEDICAL CO., LTD.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.
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