Taiwan FDA registration 3d6f64df0435d506c8f215d458b8d012
"Inofi" ureteral guide sheath
TW: “因諾斐”輸尿管導引鞘
Taiwan·Risk Class 2·INNOVEX MEDICAL CO., LTD.·Registered Apr 01, 2020 – Apr 01, 2025ExpiredRegistration details
- Analysis ID
- 3d6f64df0435d506c8f215d458b8d012
- Customs Code
- DHA09200115300
Company information
- Manufacturer
- INNOVEX MEDICAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- INNOFUTURE INTERNATIONAL INC.
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.5130 泌尿導管及其附件
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 01, 2020
- Expiry Date
- Apr 01, 2025
About this record
Access comprehensive regulatory information for "Inofi" ureteral guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d6f64df0435d506c8f215d458b8d012 and manufactured by INNOVEX MEDICAL CO., LTD.. The authorized representative in Taiwan is INNOFUTURE INTERNATIONAL INC..
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