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"Covidien" Spersmac Advanced Edition Organizational Entry and Divestiture System - Taiwan Registration aa2403d06522be9e043ccda042ee5a96

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..

This page provides complete technical specifications, regulatory compliance details. 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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aa2403d06522be9e043ccda042ee5a96
Registration Details
Taiwan FDA Registration: aa2403d06522be9e043ccda042ee5a96
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Device Details

"Covidien" Spersmac Advanced Edition Organizational Entry and Divestiture System
TW: โ€œๆŸฏๆƒ โ€ๅฒ่ฒๆ–ฏ้บฅๅ…‹้€ฒ้šŽ็‰ˆ็ต„็น”้€ฒๅ…ฅ่ˆ‡ๅ‰้›ข็ณป็ตฑ
Risk Class 2

Registration Details

aa2403d06522be9e043ccda042ee5a96

DHA05603297101

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Oct 10, 2019

Oct 10, 2029