Taiwan FDA registration c33e76106a95065c05152cead2512352

"Covidien" Rijashoul Artex tissue fusion laparoscopic instrument

TW: “柯惠”利嘉修爾亞特力士組織融合腹腔鏡器械
Taiwan flagTaiwan·Risk Class 2·COVIDIEN LLC;; COVIDIEN MEDICAL PRODUCTS (SHANGHAI) MANUFACTURING L.L.C.·Registered Oct 06, 2016 – Oct 06, 2021Cancelled
Registration details
Analysis ID
c33e76106a95065c05152cead2512352
Customs Code
DHA09200077707
Company information
Manufacturer Country
United States;;China
Authorized Representative
Taiwan Covidien Corporation Limited
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;; Chinese goods
Dates and status
Registration Date
Oct 06, 2016
Expiry Date
Oct 06, 2021
Cancellation Date
Mar 16, 2017
Cancellation information
Status
Logged out
Reason
公司歇業
About this record

Access comprehensive regulatory information for "Covidien" Rijashoul Artex tissue fusion laparoscopic instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c33e76106a95065c05152cead2512352 and manufactured by COVIDIEN LLC;; COVIDIEN MEDICAL PRODUCTS (SHANGHAI) MANUFACTURING L.L.C.. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

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