"Ouju" low-frequency therapy device
Taiwan·Risk Class 2·AND GIKEN CO., LTD., OKU FACTORY·Registered Jun 11, 2010 – Jun 11, 2015Cancelled- Analysis ID
- c3ee4b176cb14c84fd17283033031e0d
- Customs Code
- DHA00602109402
- Manufacturer
- AND GIKEN CO., LTD., OKU FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
- Intended Use
- Relieves shoulder pain and peripheral nerve paralysis, and promotes local blood circulation.
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- import
- Registration Date
- Jun 11, 2010
- Expiry Date
- Jun 11, 2015
- Cancellation Date
- Jul 31, 2018
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Ouju" 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 c3ee4b176cb14c84fd17283033031e0d and manufactured by AND GIKEN 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., OKU FACTORY, AND GIKEN 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.