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"Covidien" respirator - Taiwan Registration 512f8955bb0b929fd302f4ba380d5a72

Access comprehensive regulatory information for "Covidien" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 512f8955bb0b929fd302f4ba380d5a72 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Covidien llc;; Covidien, and 1 recent registrations in the same category. 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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512f8955bb0b929fd302f4ba380d5a72
Registration Details
Taiwan FDA Registration: 512f8955bb0b929fd302f4ba380d5a72
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Device Details

"Covidien" respirator
TW: โ€œๆŸฏๆƒ โ€ๅ‘ผๅธๅ™จ
Risk Class 2
Cancelled

Registration Details

512f8955bb0b929fd302f4ba380d5a72

DHA05602568101

Company Information

Ireland;;United States

Product Details

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

D Anesthesiology

D.5895 Continuous respirators

import

Dates and Status

Dec 31, 2013

Dec 31, 2023

Sep 21, 2022

Cancellation Information

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