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"BenQ Mitoyo" respirator tubing (unsterilized) - Taiwan Registration 1d5ece7617df5509e0e3f08edfca5c56

Access comprehensive regulatory information for "BenQ Mitoyo" respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d5ece7617df5509e0e3f08edfca5c56 and manufactured by HSINER CO., LTD.. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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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1d5ece7617df5509e0e3f08edfca5c56
Registration Details
Taiwan FDA Registration: 1d5ece7617df5509e0e3f08edfca5c56
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Device Details

"BenQ Mitoyo" respirator tubing (unsterilized)
TW: "ๆ˜ŽๅŸบไธ‰่ฑ" ๅ‘ผๅธๅ™จ็ฎก่ทฏ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

1d5ece7617df5509e0e3f08edfca5c56

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.

D Anesthesiology

D.5975 Respirator Tubing

QMS/QSD;; ๅง”่จ—่ฃฝ้€ ;; ๅœ‹็”ข

Dates and Status

Jul 24, 2012

Jul 24, 2027