Taiwan FDA registration 0af7bec1309e10fb80d961d5d2beb569

Percutaneous nerve stimulator

TW: 世延經皮神經刺激器
Taiwan flagTaiwan·Risk Class 2·WELL-LIFE HEALTHCARE LIMITED·Registered Nov 07, 2019 – Jul 21, 2021Cancelled
Registration details
Analysis ID
0af7bec1309e10fb80d961d5d2beb569
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
S&T BIOMED CO., LTD.
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
Nov 07, 2019
Expiry Date
Jul 21, 2021
Cancellation Date
Jul 21, 2023
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 Percutaneous 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 0af7bec1309e10fb80d961d5d2beb569 and manufactured by WELL-LIFE HEALTHCARE LIMITED. The authorized representative in Taiwan is S&T BIOMED CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BIO ELECTRONICS PTY LTD., AND GIKEN CO., LTD., and 2 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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