Taiwan FDA registration 3eb0a298ecad126def071e0f0fae6cb5
"Termao" Aifu microsphere
TW: “泰爾茂”籟芙微球體
Taiwan·Risk Class 3·MicroVention Europe SARL; MicroVention, Inc.·Registered May 03, 2018 – May 03, 2028ActiveRegistration details
- Analysis ID
- 3eb0a298ecad126def071e0f0fae6cb5
- Customs Code
- DHA05603076300
Company information
- Manufacturer
- MicroVention Europe SARL; MicroVention, Inc.
- Manufacturer Country
- France;;United States
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., 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.3300 動脈栓塞裝置
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- May 03, 2018
- Expiry Date
- May 03, 2028
About this record
Access comprehensive regulatory information for "Termao" Aifu microsphere in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3eb0a298ecad126def071e0f0fae6cb5 and manufactured by MicroVention Europe SARL; MicroVention, Inc.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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