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“Gemore” Transcutaneous Electrical Nerve Stimulator - Taiwan Registration cde02c5625e3c55681464e0b1e8cab00

Access comprehensive regulatory information for “Gemore” 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 cde02c5625e3c55681464e0b1e8cab00 and manufactured by Jimao Technology Co., Ltd. freshwater plant. The authorized representative in Taiwan is Jimao Technology Co., Ltd. freshwater plant.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Jimao Technology Co., Ltd. freshwater plant, 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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Registration Details
Taiwan FDA Registration: cde02c5625e3c55681464e0b1e8cab00
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Device Details

“Gemore” Transcutaneous Electrical Nerve Stimulator
TW: “吉懋”經皮神經電刺激器
Risk Class 2
MD

Registration Details

cde02c5625e3c55681464e0b1e8cab00

Ministry of Health Medical Device Manufacturing No. 004681

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

K Devices for neuroscience

K5890 Transcutaneous electrical nerve stimulator for pain relief

Produced in Taiwan, China

Dates and Status

Oct 06, 2014

Oct 06, 2024

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