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"Renova" vagus nerve stimulation therapy system program controller - Taiwan Registration cfc24e4a2257df3659a9335476030ab2

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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cfc24e4a2257df3659a9335476030ab2
Registration Details
Taiwan FDA Registration: cfc24e4a2257df3659a9335476030ab2
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Device Details

"Renova" vagus nerve stimulation therapy system program controller
TW: "็†่ซพ็" ่ฟท่ตฐ็ฅž็ถ“ๅˆบๆฟ€ๆฒป็™‚็ณป็ตฑ็จ‹ๆŽงๅ„€
Risk Class 3

Registration Details

cfc24e4a2257df3659a9335476030ab2

DHA00602305002

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

K Neuroscience

K.5820 ๆคๅ…ฅๅผๅฐ่…ฆๅˆบๆฟ€ๅ™จ

import

Dates and Status

Dec 07, 2011

Dec 07, 2026