Taiwan FDA registration aa2403d06522be9e043ccda042ee5a96
"Covidien" Spersmac Advanced Edition Organizational Entry and Divestiture System
TW: “柯惠”史貝斯麥克進階版組織進入與剝離系統
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Oct 10, 2019 – Oct 10, 2029ActiveRegistration details
- Analysis ID
- aa2403d06522be9e043ccda042ee5a96
- Customs Code
- DHA05603297101
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Oct 10, 2019
- Expiry Date
- Oct 10, 2029
About this record
Access comprehensive regulatory information for "Covidien" Spersmac Advanced Edition Organizational Entry and Divestiture System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa2403d06522be9e043ccda042ee5a96 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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