"Viaan" high-frequency oscillating breathing apparatus tubing (unsterilized) - Taiwan Registration 8551b1681890cc1f16c6af580086713e
Access comprehensive regulatory information for "Viaan" high-frequency oscillating breathing apparatus tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8551b1681890cc1f16c6af580086713e and manufactured by Vyaire Medical, Inc.. The authorized representative in Taiwan is TRANSCORE TAIWAN 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.
Device Details
Product Details
Limited to the first level identification range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.
D Anesthesiology
D.5975 Respirator Tubing
import
Dates and Status
Oct 20, 2009
Oct 20, 2024

