Taiwan FDA registration 362aa238de3b20cccc31b5a91752e8cd
"Sdio Tis" Titan guidewire
TW: “斯迪奧鈦思”泰坦導絲
Taiwan·Risk Class 2·STEREOTAXIS, INC.·Registered Aug 25, 2010 – Aug 25, 2015CancelledRegistration details
- Analysis ID
- 362aa238de3b20cccc31b5a91752e8cd
- Customs Code
- DHA00602132709
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
- Aug 25, 2010
- Expiry Date
- Aug 25, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Sdio Tis" Titan guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 362aa238de3b20cccc31b5a91752e8cd and manufactured by STEREOTAXIS, INC.. The authorized representative in Taiwan is UPWARDS BIOSYSTEMS 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