Taiwan FDA registration f9b850a4b0990c35eac88c8ee8170470
"Caudis" Enlamo balloon dilation catheter
TW: "考迪斯" 恩喇莫氣球擴張導管
Taiwan·CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.·Registered Jan 10, 2002 – Jan 10, 2007CancelledRegistration details
- Analysis ID
- f9b850a4b0990c35eac88c8ee8170470
- Customs Code
- DHA00600980202
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
- Jan 10, 2002
- Expiry Date
- Jan 10, 2007
- 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 "Caudis" Enlamo balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number f9b850a4b0990c35eac88c8ee8170470 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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