"Japanese Medical" low-frequency therapy device
Taiwan·Risk Class 2·Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd.·Registered Oct 09, 2014 – Oct 09, 2029Active- Analysis ID
- d51160b31afaeaa7edb6cbb506f7c4b9
- Customs Code
- DHA05602663805
- 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
- Oct 09, 2014
- Expiry Date
- Oct 09, 2029
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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 d51160b31afaeaa7edb6cbb506f7c4b9 and manufactured by Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd.. 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, 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.