Taiwan FDA registration 00932c2d6859136cf1a86e1b3eaa32f9
Boston Tech Internell Microelectrode Open Perfusion Defibrillation Catheter
TW: “波士頓科技”因特拉奈芙微電極開放式灌注除顫導管
Taiwan·Risk Class 3·Boston Scientific Corporation·Registered Jan 04, 2019 – Jan 04, 2029ActiveRegistration details
- Analysis ID
- 00932c2d6859136cf1a86e1b3eaa32f9
- Customs Code
- DHA05603206203
Company information
- Manufacturer
- Boston Scientific Corporation
- Manufacturer Country
- Costa Rica;;United States
- Authorized Representative
- Dutch Boston Technology Co., Ltd. Taiwan Branch
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.0008.
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jan 04, 2019
- Expiry Date
- Jan 04, 2029
About this record
Access comprehensive regulatory information for Boston Tech Internell Microelectrode Open Perfusion Defibrillation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 00932c2d6859136cf1a86e1b3eaa32f9 and manufactured by Boston Scientific Corporation. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.
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