Taiwan FDA registration 57c362abf1c1ec5e7fc03a5b29f1aabc
PHANTOM Thrombus Removing Aspiration Catheter System
TW: 惠通血栓移除抽吸管
Taiwan·Risk Class 2·MD·Endocor GmbH·Registered May 09, 2016 – May 09, 2021CancelledRegistration details
- Analysis ID
- 57c362abf1c1ec5e7fc03a5b29f1aabc
- License Form
- Ministry of Health Medical Device Import No. 028530
- Customs Code
- DHA05602853008
Company information
- Manufacturer
- Endocor GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- ITTE BIOTECHNOLOGY LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 09, 2016
- Expiry Date
- May 09, 2021
- Cancellation Date
- Aug 05, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for PHANTOM Thrombus Removing Aspiration Catheter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57c362abf1c1ec5e7fc03a5b29f1aabc and manufactured by Endocor GmbH. The authorized representative in Taiwan is ITTE BIOTECHNOLOGY LTD..
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