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"Kaiwei" non-powered, single patient use, portable suction device (unsterilized) - Taiwan Registration bcd39d32e3c8940f3999844a5748d0ec

Access comprehensive regulatory information for "Kaiwei" non-powered, single patient use, portable suction device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bcd39d32e3c8940f3999844a5748d0ec and manufactured by KAIWEI (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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Registration Details
Taiwan FDA Registration: bcd39d32e3c8940f3999844a5748d0ec
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Device Details

"Kaiwei" non-powered, single patient use, portable suction device (unsterilized)
TW: โ€œๆ„ทๅจโ€้žๅ‹•ๅŠ›ๅผ๏ผŒๅ–ฎไธ€็—…ไบบไฝฟ็”จ๏ผŒๅฏๆ”œๅธถๅผไน‹ๆŠฝๅธๅ™จๅ…ท๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

bcd39d32e3c8940f3999844a5748d0ec

DHA04600090108

Company Information

Product Details

Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".

I General, Plastic Surgery and Dermatology

I.4680 Non-motive, single patient-use, carry-on suctioning device

Input;; Chinese goods

Dates and Status

Apr 02, 2010

Apr 02, 2025