Taiwan FDA registration bed960f9d81bf3dff38fc242c8a7b8e4

"Ashokol" nosebleeds balloon (sterilized)

TW: "阿碩柯爾" 止鼻血用氣球 (滅菌)
Taiwan flagTaiwan·Risk Class 1·ARTHROCARE CORPORATION·Registered Nov 03, 2015 – Nov 03, 2025Expired
Registration details
Analysis ID
bed960f9d81bf3dff38fc242c8a7b8e4
Customs Code
DHA09401580902
Company information
Manufacturer Country
United States
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Nov 03, 2015
Expiry Date
Nov 03, 2025
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About this record

Access comprehensive regulatory information for "Ashokol" nosebleeds 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 bed960f9d81bf3dff38fc242c8a7b8e4 and manufactured by ARTHROCARE CORPORATION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ARTHROCARE CORPORATION, ArthroCare Corporation, and 2 recent registrations in the same category. 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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