Taiwan FDA registration 15a64ba6d225bd7dcefc141316316feb
"Baojian" extracorporeal shock wave lithotripter
TW: "寶健" 體外震波碎石機
Taiwan·Risk Class 2·Baojian Technology Co., Ltd. new store second factory·Registered Jun 03, 2003 – Jun 03, 2028ActiveRegistration details
- Analysis ID
- 15a64ba6d225bd7dcefc141316316feb
- Customs Code
- DHYS0500100008
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LITE-MED INC.
Product details
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- Input;; A consent form is required for each entry (a consent letter from the approved hospital clinic of the Department is required for each entry)
Dates and status
- Registration Date
- Jun 03, 2003
- Expiry Date
- Jun 03, 2028
About this record
Access comprehensive regulatory information for "Baojian" extracorporeal shock wave lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 15a64ba6d225bd7dcefc141316316feb and manufactured by Baojian Technology Co., Ltd. new store second factory. The authorized representative in Taiwan is LITE-MED INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices