“Schiller” Defibrillators with monitoring functionality - Taiwan Registration 2e301d782cc7248d24b6917a54b49de8
Access comprehensive regulatory information for “Schiller” Defibrillators with monitoring functionality in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2e301d782cc7248d24b6917a54b49de8 and manufactured by Schiller Medical. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.
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
Registration Details
2e301d782cc7248d24b6917a54b49de8
Ministry of Health Medical Device Import No. 030610
DHA05603061001
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular devices
E5310 Automated External Defibrillator
Imported from abroad
Dates and Status
Dec 07, 2017
Dec 07, 2027

