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"Fuqiang" siliceous nasal hemostatic balloon (sterilized) - Taiwan Registration 6a7c6e0ab12b2147e04598965bc2f8d6

Access comprehensive regulatory information for "Fuqiang" siliceous nasal hemostatic balloon (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6a7c6e0ab12b2147e04598965bc2f8d6 and manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. The authorized representative in Taiwan is FORTUNE MEDICAL INSTRUMENT CORP..

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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6a7c6e0ab12b2147e04598965bc2f8d6
Registration Details
Taiwan FDA Registration: 6a7c6e0ab12b2147e04598965bc2f8d6
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Device Details

"Fuqiang" siliceous nasal hemostatic balloon (sterilized)
TW: โ€œๅฏŒๅผทโ€ ็Ÿฝ่ณช้ผป่…”ๆญข่ก€ๆฐฃ็ƒ (ๆป…่Œ)
Risk Class 1

Registration Details

6a7c6e0ab12b2147e04598965bc2f8d6

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of the "Balloon for Nosebleeds (G.4100)" of the Administrative Measures for the Classification and Grading of Medical Devices.

G ENT Science

G.4100 Balloons for stopping nosebleeds

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jan 02, 2008

Jan 02, 2028