“gke” Steri-Record Package Monitoring Indicators - Taiwan Registration 5fef5e767c3a9aadf74b760ed62df251
Access comprehensive regulatory information for “gke” Steri-Record Package Monitoring Indicators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5fef5e767c3a9aadf74b760ed62df251 and manufactured by GKE-GMBH. The authorized representative in Taiwan is Yida Industrial Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GKE-GMBH, 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
5fef5e767c3a9aadf74b760ed62df251
Ministry of Health Medical Device Import No. 026126
DHA05602612604
Product Details
For details, it is Chinese approved copy of the imitation order
J General hospital and personal use equipment
J2800 Sterilization Process Indicator
Imported from abroad
Dates and Status
Apr 30, 2014
Apr 30, 2024