Taiwan FDA registration 468b08b73d9616640c7f2ef089a3e335
"Asahi Dofan balloon expansion catheter
TW: “朝日”朵凡氣球擴張導管
Taiwan·Risk Class 3·ASAHI INTECC CO., LTD. SETO FACTORY·Registered Feb 23, 2011 – Feb 23, 2021CancelledRegistration details
- Analysis ID
- 468b08b73d9616640c7f2ef089a3e335
- Customs Code
- DHA00602206701
Company information
- Manufacturer
- ASAHI INTECC CO., LTD. SETO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- This product has a dilated effect on narrowed coronary arteries during balloon dilation (PTCA) and provides dilation after positioning stents
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0005.
- Import Information
- import
Dates and status
- Registration Date
- Feb 23, 2011
- Expiry Date
- Feb 23, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Asahi Dofan balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 468b08b73d9616640c7f2ef089a3e335 and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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