"Omron" low-frequency therapy device
Taiwan·Risk Class 2·OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY·Registered Feb 23, 2019 – Feb 23, 2029Active- Analysis ID
- a56b05caadfe0e608c16f280617a426b
- Customs Code
- DHA09200098300
- Manufacturer
- OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- OMRON HEALTHCARE TAIWAN CO., LTD.
- 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
- Contract manufacturing;; Input;; Chinese goods
- Registration Date
- Feb 23, 2019
- Expiry Date
- Feb 23, 2029
- Cancellation Date
- May 10, 2024
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Access comprehensive regulatory information for "Omron" 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 a56b05caadfe0e608c16f280617a426b and manufactured by OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.;; OMRON HEALTHCARE CO., LTD., and 2 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.