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"AirLife" Ventilator tubing (NON-STERILE) - Taiwan Registration f9d91087419174ea415faad66a532980

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.

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f9d91087419174ea415faad66a532980
Registration Details
Taiwan FDA Registration: f9d91087419174ea415faad66a532980
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Device Details

"AirLife" Ventilator tubing (NON-STERILE)
TW: "ๆ„›ๆจ‚ๆดป" ๅ‘ผๅธๅ™จ็ฎก่ทฏ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f9d91087419174ea415faad66a532980

Ministry of Health Medical Device Import No. 017589

DHA09401758901

Company Information

Product Details

Limited to the first level identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.

D Devices for anesthesiology

D5975 Respirator tubing

Imported from abroad

Dates and Status

Mar 10, 2017

Mar 10, 2022