Taiwan FDA registration f9d91087419174ea415faad66a532980

"AirLife" Ventilator tubing (NON-STERILE)

TW: "愛樂活" 呼吸器管路 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.·Registered Mar 10, 2017 – Mar 10, 2022Expired
Registration details
Analysis ID
f9d91087419174ea415faad66a532980
License Form
Ministry of Health Medical Device Import No. 017589
Customs Code
DHA09401758901
Company information
Manufacturer Country
Mexico
Authorized Representative
PHOENIX INSTRUMENT BUSINESS CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5975 Respirator tubing
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 10, 2017
Expiry Date
Mar 10, 2022
About this record

Access comprehensive regulatory information for "AirLife" Ventilator tubing (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 f9d91087419174ea415faad66a532980 and manufactured by PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS CO., LTD..

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