Taiwan FDA registration 77817372b1f5e4b4c8c1d95a5576e9ff
Bayer rapid thromptom catheter set
TW: “拜耳”快捷血栓清除導管組
Taiwan·Risk Class 2·Bayer Medical Care Inc.·Registered May 01, 2009 – May 01, 2019CancelledRegistration details
- Analysis ID
- 77817372b1f5e4b4c8c1d95a5576e9ff
- Customs Code
- DHA00601982405
Company information
- Manufacturer
- Bayer Medical Care Inc.
- Manufacturer Country
- United States
- Authorized Representative
- WATTCAN INSTRUMENTS CO., 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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2009
- Expiry Date
- May 01, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Bayer rapid thromptom catheter set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77817372b1f5e4b4c8c1d95a5576e9ff and manufactured by Bayer Medical Care Inc.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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