Taiwan FDA registration 6ab64d0c3984192f15a94ee70dc32e23
"Zimmer" low-frequency therapy device (wireless)
TW: “傑邁”低周波治療儀(無線式)
Taiwan·Risk Class 2·ZMI ELECTRONICS LTD.·Registered May 05, 2023 – May 05, 2028ActiveRegistration details
- Analysis ID
- 6ab64d0c3984192f15a94ee70dc32e23
Company information
- Manufacturer
- ZMI ELECTRONICS LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ZMI ELECTRONICS LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience;;O Physical Medical Sciences
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief; O.5850 Powered Muscle Stimulator
- Import Information
- Domestic
Dates and status
- Registration Date
- May 05, 2023
- Expiry Date
- May 05, 2028
About this record
Access comprehensive regulatory information for "Zimmer" low-frequency therapy device (wireless) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ab64d0c3984192f15a94ee70dc32e23 and manufactured by ZMI ELECTRONICS LTD.. The authorized representative in Taiwan is ZMI ELECTRONICS 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.
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