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“Neurosign” IOM Stimulation Probe - Taiwan Registration ff22a04ee9971ff1fb849a6bb7075422

Access comprehensive regulatory information for “Neurosign” IOM Stimulation Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff22a04ee9971ff1fb849a6bb7075422 and manufactured by TECHNOMED EUROPE. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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ff22a04ee9971ff1fb849a6bb7075422
Registration Details
Taiwan FDA Registration: ff22a04ee9971ff1fb849a6bb7075422
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Device Details

“Neurosign” IOM Stimulation Probe
TW: “紐倫帥”刺激探頭
Risk Class 2
MD

Registration Details

ff22a04ee9971ff1fb849a6bb7075422

Ministry of Health Medical Device Import No. 035939

DHA05603593907

Company Information

Netherlands

Product Details

Details are as detailed as approved Chinese instructions

G ENT Science

G1820 Surgical neurostimulator/positioner

Imported from abroad

Dates and Status

Oct 18, 2022

Oct 18, 2027