Taiwan FDA registration 7c01c42301d82e0ad6ab8cdc62d3afdc
Bayer second-generation quick-take thrombus removal catheter
TW: “拜耳”第二代快取血栓清除導管
Taiwan·Risk Class 2·Bayer Medical Care Inc.·Registered Jun 18, 2012 – Jun 18, 2017CancelledRegistration details
- Analysis ID
- 7c01c42301d82e0ad6ab8cdc62d3afdc
- Customs Code
- DHA00602373100
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
- Jun 18, 2012
- Expiry Date
- Jun 18, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Bayer second-generation quick-take thrombus removal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7c01c42301d82e0ad6ab8cdc62d3afdc and manufactured by Bayer Medical Care Inc.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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