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“Gemore” Transcutaneous Electrical Nerve Stimulator - Taiwan Registration cf2fbb218f7aee6f12758a0d78442534

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 cf2fbb218f7aee6f12758a0d78442534 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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cf2fbb218f7aee6f12758a0d78442534
Registration Details
Taiwan FDA Registration: cf2fbb218f7aee6f12758a0d78442534
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Device Details

“Gemore” Transcutaneous Electrical Nerve Stimulator
TW: “吉懋”低週波治療器
Risk Class 2
MD

Registration Details

cf2fbb218f7aee6f12758a0d78442534

Ministry of Health Medical Device Manufacturing No. 005281

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

Apr 04, 2016

Apr 04, 2026

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