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"Kinestica" Continuous Passive Motion Device (Non-Sterile) - Taiwan Registration 3d6a2e1c54e5ec52109fd23497794253

Access comprehensive regulatory information for "Kinestica" Continuous Passive Motion Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3d6a2e1c54e5ec52109fd23497794253 and manufactured by KINESTICA D.O.O.. The authorized representative in Taiwan is SCHMIDT SCIENTIFIC TAIWAN LTD..

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3d6a2e1c54e5ec52109fd23497794253
Registration Details
Taiwan FDA Registration: 3d6a2e1c54e5ec52109fd23497794253
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Device Details

"Kinestica" Continuous Passive Motion Device (Non-Sterile)
TW: "้‡‘ๆ–ฏๆๅก" ้€ฃ็บŒๅผ่ขซๅ‹•้—œ็ฏ€ๆดปๅ‹•ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3d6a2e1c54e5ec52109fd23497794253

Ministry of Health Medical Device Import No. 019428

DHA09401942800

Company Information

Slovenia

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Continuous Passive Joint Activator (O.0006)".

o Equipment for physical medicine

O0006 Continuous Passive Joint Activator

Imported from abroad

Dates and Status

Jul 30, 2018

Jul 30, 2023