Taiwan FDA registration 7276a270cc3a74b2381a98d9bfc8a3f4

"Ouju" electrical stimulator

TW: “歐居”電刺激器
Taiwan flagTaiwan·Risk Class 2·AND GIKEN CO., LTD., OKU FACTORY·Registered Oct 15, 2015 – Oct 15, 2025Expired
Registration details
Analysis ID
7276a270cc3a74b2381a98d9bfc8a3f4
Customs Code
DHA05602781901
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)
K.5890 Transcutaneous electrical nerve stimulator for pain relief; O.5850 Powered Muscle Stimulator
Import Information
import
Dates and status
Registration Date
Oct 15, 2015
Expiry Date
Oct 15, 2025
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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 7276a270cc3a74b2381a98d9bfc8a3f4 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, 1 companies making similar products including OG Wellness Technologies CO., Ltd;;OG Wellness Technologies 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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