Pure Global

"Covidien" trocar needle - Taiwan Registration cdb5c0437d3b9af9a387a6a3c3dc3b90

Access comprehensive regulatory information for "Covidien" trocar needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cdb5c0437d3b9af9a387a6a3c3dc3b90 and manufactured by COVIDIEN LLC;; COVIDIEN IRELAND LIMITED. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
cdb5c0437d3b9af9a387a6a3c3dc3b90
Registration Details
Taiwan FDA Registration: cdb5c0437d3b9af9a387a6a3c3dc3b90
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Covidien" trocar needle
TW: "ๆŸฏๆƒ " ๅฅ—็ฎก้‡
Risk Class 2
Cancelled

Registration Details

cdb5c0437d3b9af9a387a6a3c3dc3b90

DHA00601298000

Company Information

Ireland;;United States

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Nov 15, 2005

Nov 15, 2015

Mar 16, 2017

Cancellation Information

Logged out

ๅ…ฌๅธๆญ‡ๆฅญ