Taiwan FDA registration 169ebb9aaa6ad4ed74b418c12b06db3c
"Bayer" Ascot thrombus removal catheter group
TW: “拜耳”雅士血栓清除導管組
Taiwan·Risk Class 2·Bayer Medical Care Inc.·Registered Mar 19, 2009 – Mar 19, 2019CancelledRegistration details
- Analysis ID
- 169ebb9aaa6ad4ed74b418c12b06db3c
- Customs Code
- DHA00601972401
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
- Mar 19, 2009
- Expiry Date
- Mar 19, 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" Ascot thrombus removal catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 169ebb9aaa6ad4ed74b418c12b06db3c and manufactured by Bayer Medical Care Inc.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices