"Di Cheng" respirator tubing (unsterilized) - Taiwan Registration 38c90eca11b6ead78fdbe1be5361d0af
Access comprehensive regulatory information for "Di Cheng" respirator 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 38c90eca11b6ead78fdbe1be5361d0af and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES 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.
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
Domestic
Dates and Status
Apr 06, 2009
Apr 06, 2024

