Taiwan FDA registration cf2fbb218f7aee6f12758a0d78442534

“Gemore” Transcutaneous Electrical Nerve Stimulator

TW: “吉懋”低週波治療器
Taiwan flagTaiwan·Risk Class 2·MD·Jimao Technology Co., Ltd. freshwater plant·Registered Apr 04, 2016 – Apr 04, 2026Expired
Registration details
Analysis ID
cf2fbb218f7aee6f12758a0d78442534
License Form
Ministry of Health Medical Device Manufacturing No. 005281
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
K Devices for neuroscience
Product Type (Level 2)
K5890 Transcutaneous electrical nerve stimulator for pain relief
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Apr 04, 2016
Expiry Date
Apr 04, 2026
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About this record

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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