"Ouju" low-frequency therapy device
Taiwan·Risk Class 2·OG Wellness Technologies CO., LTD., OKU FACTORY·Registered Apr 21, 2010 – Apr 21, 2020Cancelled- Analysis ID
- e51de1a175c4e51edc83621787441297
- Customs Code
- DHA00602092501
- Manufacturer
- OG Wellness Technologies CO., LTD., OKU FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
- Intended Use
- Promote local blood circulation, relieve shoulder pain and peripheral nerve paralysis.
- 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 21, 2010
- Expiry Date
- Apr 21, 2020
- Cancellation Date
- May 19, 2022
- Status
- Logged out
- Reason
- 自行鍵入
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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 e51de1a175c4e51edc83621787441297 and manufactured by OG Wellness Technologies CO., LTD., OKU FACTORY. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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