Taiwan FDA registration 8971714ff1a42bc8a144076f1fe7e2f6
“Applied” Kii Dissecting Balloon Access System
TW: “安培”腹腔鏡氣球撐開式套管
Taiwan·Risk Class 2·MD·APPLIED MEDICAL RESOURCES CORPORATION·Registered Dec 25, 2020 – Dec 25, 2025ExpiredRegistration details
- Analysis ID
- 8971714ff1a42bc8a144076f1fe7e2f6
- License Form
- Ministry of Health Medical Device Import No. 034135
- Customs Code
- DHA05603413501
Company information
- Manufacturer
- APPLIED MEDICAL RESOURCES CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 25, 2020
- Expiry Date
- Dec 25, 2025
About this record
Access comprehensive regulatory information for “Applied” Kii Dissecting Balloon Access System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8971714ff1a42bc8a144076f1fe7e2f6 and manufactured by APPLIED MEDICAL RESOURCES CORPORATION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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