Taiwan FDA registration b0aef1b0f2832ab85c52e80ae94d5746
“Penumbra” 3D Revascularization Device
TW: “彼娜波”血管重建裝置
Taiwan·Risk Class 2·MD·PENUMBRA, INC.·Registered Sep 18, 2020 – Sep 18, 2025ExpiredRegistration details
- Analysis ID
- b0aef1b0f2832ab85c52e80ae94d5746
- License Form
- Ministry of Health Medical Device Import No. 033981
- Customs Code
- DHA05603398109
Company information
- Manufacturer
- PENUMBRA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 18, 2020
- Expiry Date
- Sep 18, 2025
About this record
Access comprehensive regulatory information for “Penumbra” 3D 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 b0aef1b0f2832ab85c52e80ae94d5746 and manufactured by PENUMBRA, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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