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"Ward" non-heavy respiration respirator group (unsterilized) - Taiwan Registration dfd1808bce1f678737869514b3093cb8

Access comprehensive regulatory information for "Ward" non-heavy respiration respirator group (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfd1808bce1f678737869514b3093cb8 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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dfd1808bce1f678737869514b3093cb8
Registration Details
Taiwan FDA Registration: dfd1808bce1f678737869514b3093cb8
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Device Details

"Ward" non-heavy respiration respirator group (unsterilized)
TW: โ€œ่ฏๅพทโ€้ž้‡ๅธๅ…ฅๅผๅ‘ผๅธ้ข็ฝฉ็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

dfd1808bce1f678737869514b3093cb8

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification of "Airway Connector (D.5810)", "Air Bag (D.5320)" and "Non-re-inhaled Respirator Mask (D.5570)" in the Administrative Measures for Classification and Classification of Medical Devices.

D Anesthesiology

D.5810 Air channel connectors;; D.5570 Non-re-inhaling respirators;; D.5320 Air sacs

Domestic

Dates and Status

Oct 30, 2018

Oct 30, 2028