Taiwan FDA registration 0d3f2e7cdcc8a3896eb113cb0e7b9549
Belaz defibrillation catheter
TW: 伯拉茲除顫導管
Registration details
- Analysis ID
- 0d3f2e7cdcc8a3896eb113cb0e7b9549
- Customs Code
- DHA00600778301
Company information
- Manufacturer
- EP TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- 0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Mar 01, 1996
- Expiry Date
- Mar 01, 2001
- Cancellation Date
- Mar 02, 2005
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Belaz defibrillation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 0d3f2e7cdcc8a3896eb113cb0e7b9549 and manufactured by EP TECHNOLOGIES, INC.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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