Taiwan FDA registration dfd1808bce1f678737869514b3093cb8

"Ward" non-heavy respiration respirator group (unsterilized)

TW: “華德”非重吸入式呼吸面罩組(未滅菌)

Taiwan·Risk Class 1·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Oct 30, 2018 – Oct 30, 2028Active

Registration details

Analysis ID: dfd1808bce1f678737869514b3093cb8

Company information

Manufacturer: HEADSTAR MEDICAL PRODUCTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HEADSTAR MEDICAL PRODUCTS CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5810 Air channel connectors;; D.5570 Non-re-inhaling respirators;; D.5320 Air sacs
Import Information: Domestic

Dates and status

Registration Date: Oct 30, 2018
Expiry Date: Oct 30, 2028

About this record

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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