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"Maxell" one-piece low-frequency physiotherapy - Taiwan Registration f756fee395f7020d4ff12ada6fe2120e

Access comprehensive regulatory information for "Maxell" one-piece low-frequency physiotherapy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f756fee395f7020d4ff12ada6fe2120e and manufactured by HIVOX BIOTEK INC.. The authorized representative in Taiwan is MAXELL TAIWAN 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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f756fee395f7020d4ff12ada6fe2120e
Registration Details
Taiwan FDA Registration: f756fee395f7020d4ff12ada6fe2120e
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Device Details

"Maxell" one-piece low-frequency physiotherapy
TW: โ€œ้บฅๅ…‹่ณฝ็ˆพโ€ไธ€็‰‡ๅผไฝŽๅ‘จๆณข็†็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

f756fee395f7020d4ff12ada6fe2120e

Company Information

Taiwan, Province of China

Product Details

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

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K.5890 Transcutaneous electrical nerve stimulator for pain relief

Domestic;; Contract manufacturing

Dates and Status

May 03, 2019

Dec 10, 2020

Jul 15, 2022

Cancellation Information

Logged out

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