Taiwan FDA registration 84ee18b6bc835f43577c66df6414138e
“QXMedical” Boosting Catheter
TW: “奎克斯”布斯霆延長導管
Taiwan·Risk Class 2·MD·QXMedical, LLC·Registered Dec 07, 2020 – Dec 07, 2025ExpiredRegistration details
- Analysis ID
- 84ee18b6bc835f43577c66df6414138e
- License Form
- Ministry of Health Medical Device Import No. 034208
- Customs Code
- DHA05603420802
Company information
- Manufacturer
- QXMedical, LLC
- Manufacturer Country
- United States
- Authorized Representative
- JADE MEDICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 07, 2020
- Expiry Date
- Dec 07, 2025
About this record
Access comprehensive regulatory information for “QXMedical” Boosting Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84ee18b6bc835f43577c66df6414138e and manufactured by QXMedical, LLC. The authorized representative in Taiwan is JADE MEDICAL ENTERPRISE CO., LTD..
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