Taiwan FDA registration cfc24e4a2257df3659a9335476030ab2
"Renova" vagus nerve stimulation therapy system program controller
TW: "理諾珐" 迷走神經刺激治療系統程控儀
Taiwan·Risk Class 3·LivaNova USA, Inc.·Registered Dec 07, 2011 – Dec 07, 2026ActiveRegistration details
- Analysis ID
- cfc24e4a2257df3659a9335476030ab2
- Customs Code
- DHA00602305002
Company information
- Manufacturer
- LivaNova USA, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5820 植入式小腦刺激器
- Import Information
- import
Dates and status
- Registration Date
- Dec 07, 2011
- Expiry Date
- Dec 07, 2026
About this record
Access comprehensive regulatory information for "Renova" vagus nerve stimulation therapy system program controller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number cfc24e4a2257df3659a9335476030ab2 and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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