Taiwan FDA registration 9e8794bb2be24aeee6c2ac92f577f7fa
"Porter" cap revascularization device
TW: “波特”蓋取血管重建裝置
Taiwan·Risk Class 2·BALT EXTRUSION SAS·Registered Nov 27, 2024 – Nov 27, 2029ActiveRegistration details
- Analysis ID
- 9e8794bb2be24aeee6c2ac92f577f7fa
- Customs Code
- DHA05603766506
Company information
- Manufacturer
- BALT EXTRUSION SAS
- Manufacturer Country
- France
- Authorized Representative
- EVERMED MEDICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke
- Import Information
- import
Dates and status
- Registration Date
- Nov 27, 2024
- Expiry Date
- Nov 27, 2029
About this record
Access comprehensive regulatory information for "Porter" cap revascularization device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e8794bb2be24aeee6c2ac92f577f7fa and manufactured by BALT EXTRUSION SAS. The authorized representative in Taiwan is EVERMED MEDICAL ENTERPRISE CO., LTD..
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