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"Xingang" respirator - Taiwan Registration 598f9250ccac0a63b6d0658623475797

Access comprehensive regulatory information for "Xingang" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 598f9250ccac0a63b6d0658623475797 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 3 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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598f9250ccac0a63b6d0658623475797
Registration Details
Taiwan FDA Registration: 598f9250ccac0a63b6d0658623475797
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Device Details

"Xingang" respirator
TW: โ€œๆ–ฐๆธฏโ€ๅ‘ผๅธๅ™จ
Risk Class 2

Registration Details

598f9250ccac0a63b6d0658623475797

DHA05602641804

Company Information

Ireland;;United States

Product Details

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

D Anesthesiology

D.5895 Continuous respirators

Contract manufacturing;; input

Dates and Status

Aug 04, 2014

Aug 04, 2024

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