Taiwan FDA registration 8115739923dae6c7931d5e1a9e74668b
Sputter catheter
TW: 史賓特導管
Registration details
- Analysis ID
- 8115739923dae6c7931d5e1a9e74668b
- Customs Code
- DHA00600841108
Company information
- Manufacturer
- MEDTRONIC INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Medtronic Dingzhong Co., Ltd
Product details
- Product Type (Level 1)
- 0608 Other intensive care units and cardiac intensive care room management
- Import Information
- import
Dates and status
- Registration Date
- Sep 22, 1997
- Expiry Date
- Sep 22, 2007
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Sputter catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 8115739923dae6c7931d5e1a9e74668b and manufactured by MEDTRONIC INC.. The authorized representative in Taiwan is Taiwan Medtronic Dingzhong 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