Taiwan FDA registration 74bae2fd5672522016ec0a8b8a97a461

"Chenbo Resonance Care" transcutaneous electrical nerve stimulator

TW: “辰波共振保健”經皮神經電刺激器
Taiwan flagTaiwan·Risk Class 2·Jinshangda Technology Co., Ltd. Sanhe Road Factory·Registered Mar 04, 2013 – Mar 04, 2018Cancelled
Registration details
Analysis ID
74bae2fd5672522016ec0a8b8a97a461
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
TAIWAN RESONANT WAVES RESEARCH CORP.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
K Neuroscience
Product Type (Level 2)
K.5890 Transcutaneous electrical nerve stimulator for pain relief
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Mar 04, 2013
Expiry Date
Mar 04, 2018
Cancellation Date
Nov 19, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Chenbo Resonance Care" transcutaneous electrical nerve stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74bae2fd5672522016ec0a8b8a97a461 and manufactured by Jinshangda Technology Co., Ltd. Sanhe Road Factory. The authorized representative in Taiwan is TAIWAN RESONANT WAVES RESEARCH CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GOLDENSUNDA TECHNOLOGY CO., LTD., 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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