Taiwan FDA registration 5cd24fa4db95ddbd436218f3ebf12ea2

"Ouju" vector interference therapy instrument

TW: “歐居”向量干擾治療儀
Taiwan flagTaiwan·Risk Class 2·OG Wellness Technologies Co., Ltd. Oku Factory·Registered May 13, 2010 – May 13, 2020Cancelled
Registration details
Analysis ID
5cd24fa4db95ddbd436218f3ebf12ea2
Customs Code
DHA00602102506
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)
o Physical Medical Sciences
Product Type (Level 2)
O.5850 5850.
Import Information
import
Dates and status
Registration Date
May 13, 2010
Expiry Date
May 13, 2020
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Ouju" vector interference therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5cd24fa4db95ddbd436218f3ebf12ea2 and manufactured by 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, 1 companies making similar products including AND GIKEN CO., LTD., OKU 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.

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