Taiwan FDA registration 51f21d45c9f20608dbcc6a4dae202aba
"Caudis" Fran chronic total occlusive catheter
TW: “考迪斯” 弗朗慢性全阻塞導管
Taiwan·Risk Class 2·CORDIS CORPORATION·Registered May 30, 2011 – May 30, 2016CancelledRegistration details
- Analysis ID
- 51f21d45c9f20608dbcc6a4dae202aba
- Customs Code
- DHA00602232408
Company information
- Manufacturer
- CORDIS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- May 30, 2011
- Expiry Date
- May 30, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Caudis" Fran chronic total occlusive catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51f21d45c9f20608dbcc6a4dae202aba and manufactured by CORDIS CORPORATION. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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