Taiwan FDA registration f9d91087419174ea415faad66a532980
"AirLife" Ventilator tubing (NON-STERILE)
TW: "愛樂活" 呼吸器管路 (未滅菌)
Registration details
- Analysis ID
- f9d91087419174ea415faad66a532980
- License Form
- Ministry of Health Medical Device Import No. 017589
- Customs Code
- DHA09401758901
Company information
- Manufacturer
- PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.
- 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..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices