"Gibeo" electrotherapy instrument
Taiwan·Risk Class 2·GBO MEDIZINTECHNIK AG.·Registered Jan 09, 2012 – Jan 09, 2022Cancelled- Analysis ID
- 581263714d4d9c9176f87451c6f8e083
- Customs Code
- DHA00602318502
- Manufacturer
- GBO MEDIZINTECHNIK AG.
- Manufacturer Country
- Germany
- Authorized Representative
- DYNO-TEC TECHNOLOGY INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5850 5850.
- Import Information
- import
- Registration Date
- Jan 09, 2012
- Expiry Date
- Jan 09, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.