Fadia Automation Instrument Series (Non-Sterile) - Taiwan Registration b5230e50216b7f656999cf5248662454
Access comprehensive regulatory information for Fadia Automation Instrument Series (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 b5230e50216b7f656999cf5248662454 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN 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
It is limited to the first level of identification of the classification and grading management of medical devices "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)".
A Clinical chemistry and clinical toxicology
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
import
Dates and Status
Dec 24, 2024
Oct 31, 2026

