Taiwan FDA registration 4cde04d27f9df4a74e0a58041b10b776
"Asahi" stage percutaneous coronary angioplasty guide tube
TW: "朝日" 階段經皮冠狀動脈成型術導引導管
Taiwan·ASAHI INTECC CO., LTD. SETO FACTORY·Registered Apr 04, 2005 – Apr 04, 2010CancelledRegistration details
- Analysis ID
- 4cde04d27f9df4a74e0a58041b10b776
- Customs Code
- DHA00601114803
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
- Apr 04, 2005
- Expiry Date
- Apr 04, 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" stage percutaneous coronary angioplasty guide tube in Taiwan's medical device market through Pure Global AI's free database. is registered under number 4cde04d27f9df4a74e0a58041b10b776 and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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