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"Covidien" thin and light implantable drug delivery system - Taiwan Registration e8ccac28ffbc18b1e7ed02461ae44113

Access comprehensive regulatory information for "Covidien" thin and light implantable drug delivery system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8ccac28ffbc18b1e7ed02461ae44113 and manufactured by COVIDIEN LLC;; COVID. 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.

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e8ccac28ffbc18b1e7ed02461ae44113
Registration Details
Taiwan FDA Registration: e8ccac28ffbc18b1e7ed02461ae44113
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Device Details

"Covidien" thin and light implantable drug delivery system
TW: โ€œๆŸฏๆƒ โ€่ผ•่–„ๅž‹ๆคๅ…ฅๅผ้‡‹่—ฅ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e8ccac28ffbc18b1e7ed02461ae44113

DHA00602372202

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J.5965 Subcutaneous implantable intravascular injection port and guide

import

Dates and Status

Jul 27, 2012

Jul 01, 2016

Jun 20, 2016

Cancellation Information

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