Taiwan FDA registration 1201c89bda83c77cd47fc5c859d8af1a

"Chenbo Resonance Care" transcutaneous electrical nerve stimulator

TW: “辰波共振保健”經皮神經電刺激器
Taiwan flagTaiwan·Risk Class 2·GOLDENSUNDA TECHNOLOGY CO., LTD.·Registered Aug 08, 2018 – Aug 08, 2028Active
Registration details
Analysis ID
1201c89bda83c77cd47fc5c859d8af1a
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
TAIWAN RESONANT WAVES RESEARCH CORP.
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;; Contract manufacturing
Dates and status
Registration Date
Aug 08, 2018
Expiry Date
Aug 08, 2028
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About this record

Access comprehensive regulatory information for "Chenbo Resonance Care" 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 1201c89bda83c77cd47fc5c859d8af1a and manufactured by GOLDENSUNDA TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is TAIWAN RESONANT WAVES RESEARCH CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Jinshangda Technology Co., Ltd. Sanhe Road Factory, and 1 recent registrations in the same category. 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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