Taiwan FDA registration 931654fc6f2b7700ca8378f18dc3db8f
"Bertie" thrombus clearance duct
TW: "柏蒂" 血栓清除導管
Taiwan·Risk Class 2·Bioptimal International Pte. Ltd.·Registered Feb 01, 1999 – Feb 01, 2029ActiveRegistration details
- Analysis ID
- 931654fc6f2b7700ca8378f18dc3db8f
- Customs Code
- DHA00600901505
Company information
- Manufacturer
- Bioptimal International Pte. Ltd.
- Manufacturer Country
- Singapore
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- 0608 Other intensive care units and cardiac intensive care room management
- Import Information
- import
Dates and status
- Registration Date
- Feb 01, 1999
- Expiry Date
- Feb 01, 2029
About this record
Access comprehensive regulatory information for "Bertie" thrombus clearance duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 931654fc6f2b7700ca8378f18dc3db8f and manufactured by Bioptimal International Pte. Ltd.. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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