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"Covidien" respirator - Taiwan Registration 8a30fe27cc70d94847bb36aa2301d60d

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 8a30fe27cc70d94847bb36aa2301d60d 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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8a30fe27cc70d94847bb36aa2301d60d
Registration Details
Taiwan FDA Registration: 8a30fe27cc70d94847bb36aa2301d60d
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Device Details

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

Registration Details

8a30fe27cc70d94847bb36aa2301d60d

DHA00602351201

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

May 24, 2012

May 24, 2022

Apr 12, 2024

Cancellation Information

Logged out

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