"Delfi" Pneumatic tourniquet (Non-Sterile) - Taiwan Registration 660aface7676deae676c60e73e9b0911
Access comprehensive regulatory information for "Delfi" Pneumatic tourniquet (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 660aface7676deae676c60e73e9b0911 and manufactured by DELFI MEDICAL INNOVATIONS INC.. The authorized representative in Taiwan is MEDEPOT CO., LTD.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DELFI MEDICAL INNOVATIONS INC., and 1 recent registrations in the same category. 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
Registration Details
660aface7676deae676c60e73e9b0911
Ministry of Health Medical Device Import No. 018427
DHA09401842703
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Inflatable Tourniquet (I.5910)".
I General and plastic surgical devices
I5910 Inflatable tourniquet
Imported from abroad
Dates and Status
Oct 19, 2017
Oct 19, 2022

