Taiwan FDA registration 1689648a25347212b685336a1bdf985d
"Chaoyang" transcutaneous electrical nerve stimulator
TW: “朝揚”經皮神經電刺激器
Registration details
- Analysis ID
- 1689648a25347212b685336a1bdf985d
- Customs Code
- DHY00500269501
Company information
- Manufacturer
- Chaoyang Plastic Factory Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Chaoyang Plastic Factory Co., Ltd
Product details
- Intended Use
- Relieves shoulder pain and peripheral nerve paralysis, and promotes local blood circulation.
- 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
- May 07, 2009
- Expiry Date
- May 07, 2029
About this record
Access comprehensive regulatory information for "Chaoyang" transcutaneous electrical nerve stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1689648a25347212b685336a1bdf985d and manufactured by Chaoyang Plastic Factory Co., Ltd. The authorized representative in Taiwan is Chaoyang Plastic Factory Co., Ltd.
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