Taiwan FDA registration c1a89609a63f0c267c47954400a9c33e
"Hanwo" Ruyi Low Frequency Therapy Device
TW: "翰沃" 如意貼低周波治療器
Taiwan·Risk Class 2·HIVOX BIOTEK INC.·Registered Oct 04, 2005 – Oct 04, 2020CancelledRegistration details
- Analysis ID
- c1a89609a63f0c267c47954400a9c33e
- Customs Code
- DHY00500150109
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 04, 2005
- Expiry Date
- Oct 04, 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" Ruyi 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 c1a89609a63f0c267c47954400a9c33e and manufactured by HIVOX BIOTEK INC.. The authorized representative in Taiwan is HIVOX BIOTEK INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices