Taiwan FDA registration a0617e24350b46f589d4d0b2ebc3913b
"Weidekang" gastrointestinal biliary dilation balloon catheter
TW: “唯德康”胃腸膽道擴張氣球導管
Taiwan·Risk Class 2·JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.·Registered Oct 25, 2021 – Oct 25, 2026ActiveRegistration details
- Analysis ID
- a0617e24350b46f589d4d0b2ebc3913b
- Customs Code
- DHA09200125903
Company information
- Manufacturer Country
- China
- Authorized Representative
- CHINA SPRING TRADING 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.5010 膽管用導管及其附件;; H.5365 食道擴張器
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Oct 25, 2021
- Expiry Date
- Oct 25, 2026
About this record
Access comprehensive regulatory information for "Weidekang" gastrointestinal biliary dilation balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0617e24350b46f589d4d0b2ebc3913b and manufactured by JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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