Taiwan FDA registration 6a7c6e0ab12b2147e04598965bc2f8d6

"Fuqiang" siliceous nasal hemostatic balloon (sterilized)

TW: “富強” 矽質鼻腔止血氣球 (滅菌)

Taiwan·Risk Class 1·FORTUNE MEDICAL INSTRUMENT CORP.·Registered Jan 02, 2008 – Jan 02, 2028Active

Registration details

Analysis ID: 6a7c6e0ab12b2147e04598965bc2f8d6

Company information

Manufacturer: FORTUNE MEDICAL INSTRUMENT CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FORTUNE MEDICAL INSTRUMENT CORP.

Product details

Intended Use: 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.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4100 Balloons for stopping nosebleeds
Import Information: 國產;; QMS/QSD

Dates and status

Registration Date: Jan 02, 2008
Expiry Date: Jan 02, 2028

About this record

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..

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