Taiwan FDA registration 983a9a63eca233790d89a2b4d3a445aa
"Asahi" does not need a guide tube for percutaneous coronary angioplasty
TW: “朝日”無需導引鞘水漾經皮冠狀動脈成型術導引導管
Taiwan·Risk Class 2·ASAHI INTECC CO., LTD. SETO FACTORY·Registered Apr 01, 2008 – Apr 01, 2023ExpiredRegistration details
- Analysis ID
- 983a9a63eca233790d89a2b4d3a445aa
- Customs Code
- DHA00601876204
Company information
- Manufacturer
- ASAHI INTECC CO., LTD. SETO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Apr 01, 2008
- Expiry Date
- Apr 01, 2023
About this record
Access comprehensive regulatory information for "Asahi" does not need a guide tube for percutaneous coronary angioplasty in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 983a9a63eca233790d89a2b4d3a445aa and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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