Taiwan FDA registration f426172125026d35d3504fa07f17c4d7
"Weidekang" non-vascular luminal guide wire
TW: “唯德康”非血管腔道導引線
Taiwan·Risk Class 2·JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.·Registered Nov 17, 2020 – Nov 17, 2025ExpiredRegistration details
- Analysis ID
- f426172125026d35d3504fa07f17c4d7
- Customs Code
- DHA09200117500
Company information
- Manufacturer Country
- China
- Authorized Representative
- CHINA SPRING TRADING 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
- Nov 17, 2020
- Expiry Date
- Nov 17, 2025
About this record
Access comprehensive regulatory information for "Weidekang" non-vascular luminal guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f426172125026d35d3504fa07f17c4d7 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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