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"Michael Air" non-powered, single-patient, portable suction device (unsterilized) - Taiwan Registration f4dedcf0cdef738ebf7a7681a94b6099

Access comprehensive regulatory information for "Michael Air" non-powered, single-patient, 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 f4dedcf0cdef738ebf7a7681a94b6099 and manufactured by MicroAire Surgical Instruments, LLC. The authorized representative in Taiwan is ACL BIOMEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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f4dedcf0cdef738ebf7a7681a94b6099
Registration Details
Taiwan FDA Registration: f4dedcf0cdef738ebf7a7681a94b6099
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Device Details

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

Registration Details

f4dedcf0cdef738ebf7a7681a94b6099

DHA04401080107

Company Information

United States

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

import

Dates and Status

Sep 05, 2011

Sep 05, 2026