Taiwan FDA registration f756fee395f7020d4ff12ada6fe2120e
"Maxell" one-piece low-frequency physiotherapy
TW: “麥克賽爾”一片式低周波理療器
Taiwan·Risk Class 2·HIVOX BIOTEK INC.·Registered May 03, 2019 – Dec 10, 2020CancelledRegistration details
- Analysis ID
- f756fee395f7020d4ff12ada6fe2120e
Company information
- Manufacturer
- HIVOX BIOTEK INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MAXELL TAIWAN 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.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- May 03, 2019
- Expiry Date
- Dec 10, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
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..
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