Taiwan FDA registration 66954fe4d323ec52aa64fdd56c8f4b9e

"Ouju" electrical stimulator

TW: “歐居”電刺激器
Taiwan flagTaiwan·Risk Class 2·OG Wellness Technologies CO., Ltd;;OG Wellness Technologies CO., LTD., OKU FACTORY·Registered Feb 16, 2019 – Feb 16, 2029Active
Registration details
Analysis ID
66954fe4d323ec52aa64fdd56c8f4b9e
Customs Code
DHA05603225402
Company information
Manufacturer Country
Japan
Authorized Representative
AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
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
Dates and status
Registration Date
Feb 16, 2019
Expiry Date
Feb 16, 2029
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About this record

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.

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