Taiwan FDA registration f943b1c51bfc349b3a4d2a769cd0bb2c
"Asahi" quick-swap percutaneous coronary angioplasty catheter
TW: "朝日" 快速抽換式經皮冠狀動脈血管成型術導管
Taiwan·ASAHI INTECC CO., LTD. SETO FACTORY·Registered Jun 22, 2005 – Jun 22, 2010CancelledRegistration details
- Analysis ID
- f943b1c51bfc349b3a4d2a769cd0bb2c
- Customs Code
- DHA00601155302
Company information
- Manufacturer
- ASAHI INTECC CO., LTD. SETO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Jun 22, 2005
- Expiry Date
- Jun 22, 2010
- Cancellation Date
- Nov 09, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Asahi" quick-swap percutaneous coronary angioplasty catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number f943b1c51bfc349b3a4d2a769cd0bb2c and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. 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