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"Carefusion" Ventilator tubing (Non-Sterile) - Taiwan Registration ededaaa9f773a25eb7edb5b5d8b76904

Access comprehensive regulatory information for "Carefusion" 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 ededaaa9f773a25eb7edb5b5d8b76904 and manufactured by CAREFUSION. The authorized representative in Taiwan is BIOSYSTEMS INC..

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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ededaaa9f773a25eb7edb5b5d8b76904
Registration Details
Taiwan FDA Registration: ededaaa9f773a25eb7edb5b5d8b76904
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Device Details

"Carefusion" Ventilator tubing (Non-Sterile)
TW: "ๅก็ˆพ่ฒป"ๅ‘ผๅธๅ™จ็ฎก่ทฏ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ededaaa9f773a25eb7edb5b5d8b76904

Ministry of Health Medical Device Import No. 018816

DHA09401881601

Company Information

Mexico

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

Feb 12, 2018

Feb 12, 2023