Taiwan FDA registration 5ed018b238482c33005241c5cbbebf92
Onepais percutaneous puncture of the coronary artery dilation catheter
TW: 歐尼派司經皮穿刺冠狀動脈擴張導管
Taiwan·CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.·Registered Nov 18, 1998 – Nov 18, 2003CancelledRegistration details
- Analysis ID
- 5ed018b238482c33005241c5cbbebf92
- Customs Code
- DHA00600893200
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)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Nov 18, 1998
- Expiry Date
- Nov 18, 2003
- Cancellation Date
- Jul 20, 2007
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Onepais percutaneous puncture of the coronary artery dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 5ed018b238482c33005241c5cbbebf92 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.
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