Taiwan FDA registration edba4c311d11559235d83acac8b6a6b6
"Hanwo" one-piece electronic low-frequency physiotherapy
TW: “翰沃”一片式電子低週波理療器
Registration details
- Analysis ID
- edba4c311d11559235d83acac8b6a6b6
- Customs Code
- DHY00500315602
Company information
- Manufacturer
- HIVOX BIOTEK INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HIVOX BIOTEK INC.
Product details
- Intended Use
- Promote local blood circulation, relieve shoulder pain and peripheral nerve paralysis.
- 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
- Dec 10, 2010
- Expiry Date
- Dec 10, 2025
About this record
Access comprehensive regulatory information for "Hanwo" one-piece electronic 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 edba4c311d11559235d83acac8b6a6b6 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.
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