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"Filisco" rigid laryngoscope (sterilized) - Taiwan Registration f91567f06c1fb8223dce79bd3944aacf

Access comprehensive regulatory information for "Filisco" rigid laryngoscope (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f91567f06c1fb8223dce79bd3944aacf and manufactured by FLEXICARE MEDICAL LIMITED.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.

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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f91567f06c1fb8223dce79bd3944aacf
Registration Details
Taiwan FDA Registration: f91567f06c1fb8223dce79bd3944aacf
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Device Details

"Filisco" rigid laryngoscope (sterilized)
TW: "่ฒๅŠ›ๆ–ฏๅฏ" ็กฌๅผๅ–‰้ ญ้ก (ๆป…่Œ)
Risk Class 1

Registration Details

f91567f06c1fb8223dce79bd3944aacf

DHA09402204300

Company Information

United Kingdom

Product Details

Limited to the first level identification range of the "rigid laryngoscope (D.5540)" of the Measures for the Classification and Grading Management of Medical Devices.

D Anesthesiology

D.5540 Rigid laryngoscope

Input;; QMS/QSD

Dates and Status

Oct 19, 2020

Oct 19, 2025