"Omron" low-frequency therapy device
Taiwan·Risk Class 2·OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.;; OMRON HEALTHCARE CO., LTD.·Registered May 17, 2024 – May 17, 2029Active- Analysis ID
- 2dee346638420ac0d04561dc916134ea
- Customs Code
- DHA05603718008
- Manufacturer Country
- Japan;;Viet Nam
- Authorized Representative
- OMRON HEALTHCARE TAIWAN CO., LTD.
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- import
- Registration Date
- May 17, 2024
- Expiry Date
- May 17, 2029
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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 2dee346638420ac0d04561dc916134ea and manufactured by OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.;; OMRON HEALTHCARE CO., LTD.. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY, 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.