Taiwan FDA registration a9763891e7b54d39dbcf80303bf9a735

"Headstar" Airway connector (Non-sterile)

TW: "華德" 氣道連接器 (未滅菌)

Taiwan·Risk Class 1·MD·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Oct 01, 2018 – Oct 01, 2028Active

Registration details

Analysis ID: a9763891e7b54d39dbcf80303bf9a735
License Form: Ministry of Health Medical Device Manufacturing No. 007455

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: Limited to the first level identification range of the "Airway Connector (D.5810)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5810 airway connector
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2018
Expiry Date: Oct 01, 2028

About this record

Access comprehensive regulatory information for "Headstar" Airway connector (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a9763891e7b54d39dbcf80303bf9a735 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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