Taiwan FDA registration 6205d20a8bba7265f66ca0cca9af697f
"Hanwo" watch-type low-frequency therapy device
TW: "翰沃" 手錶型低週波治療器
Taiwan·Risk Class 2·HIVOX BIOTEK INC.·Registered Oct 18, 2005 – Oct 18, 2020CancelledRegistration details
- Analysis ID
- 6205d20a8bba7265f66ca0cca9af697f
- Customs Code
- DHY00500153704
Company information
- Manufacturer
- HIVOX BIOTEK INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HIVOX BIOTEK INC.
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
Dates and status
- Registration Date
- Oct 18, 2005
- Expiry Date
- Oct 18, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hanwo" watch-type low-frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6205d20a8bba7265f66ca0cca9af697f and manufactured by HIVOX BIOTEK INC.. The authorized representative in Taiwan is HIVOX BIOTEK INC..
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