Taiwan FDA registration be5bed06bceff3756694be89c0415069
"Sdio Tis" Pegesas guidewire
TW: “斯迪奧鈦思”佩格薩斯導絲
Taiwan·Risk Class 2·STEREOTAXIS, INC.·Registered Sep 07, 2010 – Sep 07, 2020CancelledRegistration details
- Analysis ID
- be5bed06bceff3756694be89c0415069
- Customs Code
- DHA00602144107
Company information
- Manufacturer
- STEREOTAXIS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- UPWARDS BIOSYSTEMS 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.1330 Catheter Guide Wires
- Import Information
- import
Dates and status
- Registration Date
- Sep 07, 2010
- Expiry Date
- Sep 07, 2020
- 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 "Sdio Tis" Pegesas guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be5bed06bceff3756694be89c0415069 and manufactured by STEREOTAXIS, INC.. The authorized representative in Taiwan is UPWARDS BIOSYSTEMS LTD..
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