“Bimini” Puregraft System - Taiwan Registration a5a1cef3ad83855350d5ddb50605d90f

Access comprehensive regulatory information for “Bimini” Puregraft System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5a1cef3ad83855350d5ddb50605d90f and manufactured by Bimini Health Tech. The authorized representative in Taiwan is ACL BIOMEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Bimini Health Tech, 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.