Taiwan FDA registration 5677e3e93c8aea51037bff65eb9dd8f3

"Ward" Venturi Mask Set (Unsterilized)

TW: “華德”Venturi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: 5677e3e93c8aea51037bff65eb9dd8f3

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)" and "Venturi Mask (D.5600)" in the Administrative Measures for the Classification and Classification of Medical Devices.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5600 Venturi面罩;; D.5810 氣道連接器
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" Venturi Mask Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5677e3e93c8aea51037bff65eb9dd8f3 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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