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"Gibeo" electrotherapy instrument - Taiwan Registration cc2362c8b637d418c97808158e1d3bf4

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 cc2362c8b637d418c97808158e1d3bf4 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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cc2362c8b637d418c97808158e1d3bf4
Registration Details
Taiwan FDA Registration: cc2362c8b637d418c97808158e1d3bf4
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Device Details

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

Registration Details

cc2362c8b637d418c97808158e1d3bf4

DHA00602318601

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

o Physical Medical Sciences

O.5850 5850.

import

Dates and Status

Jan 10, 2012

Jan 10, 2027

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