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"Gibeo" electrotherapy instrument - Taiwan Registration ca2ae7a20470c6afa08cb4a93caf4d43

Access comprehensive regulatory information for "Gibeo" electrotherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca2ae7a20470c6afa08cb4a93caf4d43 and manufactured by GBO MEDIZINTECHNIK AG.. The authorized representative in Taiwan is DYNO-TEC TECHNOLOGY INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GBO MEDIZINTECHNIK AG., 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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ca2ae7a20470c6afa08cb4a93caf4d43
Registration Details
Taiwan FDA Registration: ca2ae7a20470c6afa08cb4a93caf4d43
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Device Details

"Gibeo" electrotherapy instrument
TW: โ€œๅ‰่ฒๆญโ€้›ป็™‚ๅ„€
Risk Class 2

Registration Details

ca2ae7a20470c6afa08cb4a93caf4d43

DHA05603530301

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience;;O Physical Medical Sciences

K.5890 Transcutaneous electrical nerve stimulator for pain relief; O.5850 Powered Muscle Stimulator

import

Dates and Status

Feb 14, 2022

Feb 14, 2027

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