"Japanese Medical" low-frequency therapy device
Taiwan·Risk Class 2·NIHON MEDIX CO., LTD. KASHIWA FACTORY·Registered Apr 01, 2013 – Apr 01, 2028Active- Analysis ID
- 4dae66c776169e81c2f1f0ff9ed4a82e
- Customs Code
- DHA00602483606
- Manufacturer
- NIHON MEDIX CO., LTD. KASHIWA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- CROWNMED ENTERPRISE 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
- import
- Registration Date
- Apr 01, 2013
- Expiry Date
- Apr 01, 2028
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Access comprehensive regulatory information for "Japanese Medical" 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 4dae66c776169e81c2f1f0ff9ed4a82e and manufactured by NIHON MEDIX CO., LTD. KASHIWA FACTORY. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd., 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.