Taiwan FDA registration 5504a51f77f4ac21743102037d75d23d
"Boston Tech" Stinger defibrillation electrode catheter
TW: “波士頓科技” 史汀格除顫電極導管
Taiwan·Risk Class 3·Boston Scientific Corporation;; C.R. BARD, INC.·Registered Oct 02, 2002 – Oct 02, 2022CancelledRegistration details
- Analysis ID
- 5504a51f77f4ac21743102037d75d23d
- Customs Code
- DHA00601009503
Company information
- Manufacturer
- Boston Scientific Corporation;; C.R. BARD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Dutch Boston Technology Co., Ltd. Taiwan Branch
Product details
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Oct 02, 2002
- Expiry Date
- Oct 02, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Boston Tech" Stinger defibrillation electrode catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5504a51f77f4ac21743102037d75d23d and manufactured by Boston Scientific Corporation;; C.R. BARD, INC.. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.
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