Taiwan FDA registration c294d16561be3df71971688a5c910c9e
6F Codice hydrolytic thrombus removal duct
TW: ６Ｆ 考迪斯水解型血栓清除導管
Taiwan·CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.·Registered Dec 20, 1997 – Dec 20, 2002CancelledRegistration details
- Analysis ID
- c294d16561be3df71971688a5c910c9e
- Customs Code
- DHAS0600849002
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
- Intended Use
- Vacuum.
- Product Type (Level 1)
- 0600 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Dec 20, 1997
- Expiry Date
- Dec 20, 2002
- 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 6F Codice hydrolytic thrombus removal duct in Taiwan's medical device market through Pure Global AI's free database. is registered under number c294d16561be3df71971688a5c910c9e 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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