Taiwan FDA registration 008d6402e697708ad292161bc9d33d09
"Caudix" Akwaia T3 coronary artery dilation catheter
TW: "考迪斯" 阿葵亞T3冠狀動脈擴張導管
Taiwan·CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.·Registered Apr 23, 2003 – Apr 23, 2008CancelledRegistration details
- Analysis ID
- 008d6402e697708ad292161bc9d33d09
- Customs Code
- DHA00601028100
Company information
- Manufacturer
- CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.
- Manufacturer Country
- Netherlands
- Authorized Representative
- Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch
Product details
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Apr 23, 2003
- Expiry Date
- Apr 23, 2008
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Caudix" Akwaia T3 coronary artery dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 008d6402e697708ad292161bc9d33d09 and manufactured by CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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