"Delfi" Pneumatic tourniquet (Non-Sterile) - Taiwan Registration 6bfa75a6302f8c63dbcf20c07aca3e86
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 6bfa75a6302f8c63dbcf20c07aca3e86 and manufactured by DELFI MEDICAL INNOVATIONS INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN 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
6bfa75a6302f8c63dbcf20c07aca3e86
Ministry of Health Medical Device Import No. 015370
DHA09401537001
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
Jun 23, 2015
Jun 23, 2025

