Taiwan FDA registration d2ab06a194322a826a5b56338350f154
“Penumbra” Penumbra System
TW: “彼娜波”彼娜波系統
Taiwan·Risk Class 2·MD·Penumbra, Inc.·Registered Sep 10, 2014 – Sep 10, 2024ExpiredRegistration details
- Analysis ID
- d2ab06a194322a826a5b56338350f154
- License Form
- Ministry of Health Medical Device Import No. 026556
- Customs Code
- DHA05602655603
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 10, 2014
- Expiry Date
- Sep 10, 2024
About this record
Access comprehensive regulatory information for “Penumbra” Penumbra System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2ab06a194322a826a5b56338350f154 and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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