Taiwan FDA registration d3f2fd6616a1241ed333a958a0dda4f8

"Asukor" otolaryngology with gasification rods

TW: “阿碩柯爾”耳鼻喉科用氣化棒
Taiwan flagTaiwan·Risk Class 2·ArthroCare Corporation·Registered Mar 09, 2018 – Mar 09, 2028Active
Registration details
Analysis ID
d3f2fd6616a1241ed333a958a0dda4f8
Customs Code
DHA05603095404
Company information
Manufacturer Country
Costa Rica;;United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Mar 09, 2018
Expiry Date
Mar 09, 2028
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About this record

Access comprehensive regulatory information for "Asukor" otolaryngology with gasification rods in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3f2fd6616a1241ed333a958a0dda4f8 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, 1 companies making similar products including 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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