“GE” Probe for medical use - Taiwan Registration 3e237a1f205c4204238ec039ed90a7cf

Access comprehensive regulatory information for “GE” Probe for medical use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e237a1f205c4204238ec039ed90a7cf and manufactured by GE Healthcare Japan Corporation. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

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.