Taiwan FDA registration 7d960030ef211a0e7b1f5485677a0e4d
“UNIPAD” neckare TENS device
TW: “優尼帕德”頸掛型低周波治療器
Taiwan·Risk Class 2·MD·HIVOX BIOTEK INC.·Registered Aug 21, 2021 – Aug 21, 2026ActiveRegistration details
- Analysis ID
- 7d960030ef211a0e7b1f5485677a0e4d
- License Form
- Ministry of Health Medical Device Manufacturing No. 007177
Company information
- Manufacturer
- HIVOX BIOTEK INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HIVOX BIOTEK INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 21, 2021
- Expiry Date
- Aug 21, 2026
About this record
Access comprehensive regulatory information for “UNIPAD” neckare TENS device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d960030ef211a0e7b1f5485677a0e4d and manufactured by HIVOX BIOTEK INC.. The authorized representative in Taiwan is HIVOX BIOTEK INC..
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