"Ouju" electrical stimulator
- Analysis ID
- 66954fe4d323ec52aa64fdd56c8f4b9e
- Customs Code
- DHA05603225402
- Manufacturer Country
- Japan
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience;;O Physical Medical Sciences
- Product Type (Level 2)
- O.5850 Powered Muscle Stimulator;; K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- import
- Registration Date
- Feb 16, 2019
- Expiry Date
- Feb 16, 2029
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Access comprehensive regulatory information for "Ouju" electrical stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66954fe4d323ec52aa64fdd56c8f4b9e and manufactured by OG Wellness Technologies CO., Ltd;;OG Wellness Technologies CO., LTD., OKU FACTORY. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including OG Wellness Technologies CO., Ltd;;OG Wellness Technologies CO., LTD., OKU FACTORY, AND GIKEN CO., LTD., OKU FACTORY, 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.