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"Gibeo" electrotherapy instrument - Taiwan Registration 581263714d4d9c9176f87451c6f8e083

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 581263714d4d9c9176f87451c6f8e083 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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581263714d4d9c9176f87451c6f8e083
Registration Details
Taiwan FDA Registration: 581263714d4d9c9176f87451c6f8e083
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Device Details

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

Registration Details

581263714d4d9c9176f87451c6f8e083

DHA00602318502

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 09, 2012

Jan 09, 2022

Apr 12, 2024

Cancellation Information

Logged out

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