Kiromi IR Correction Solution II - Taiwan Registration 3696cda6f3c1e182573ab8a076619de4
Access comprehensive regulatory information for Kiromi IR Correction Solution II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3696cda6f3c1e182573ab8a076619de4 and manufactured by SYNERMED INTERNATIONAL INC.. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..
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
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A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
import
Dates and Status
Jun 30, 2006
Jun 30, 2011
Nov 26, 2012
Cancellation Information
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