"Singular" oximetry - Taiwan Registration 2353d51cf467dc4e2691e769a920b7f8
Access comprehensive regulatory information for "Singular" oximetry in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2353d51cf467dc4e2691e769a920b7f8 and manufactured by GE HEALTHCARE-CRITIKON DE MEXICO S. DE R.L. DE C.V.; GE Medical Systems Information Technologies. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GE HEALTHCARE FINLAND OY, 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
2353d51cf467dc4e2691e769a920b7f8
DHA00601382006
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
import
Dates and Status
Dec 16, 2005
Dec 16, 2015
Apr 25, 2018
Cancellation Information
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