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“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.

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2e301d782cc7248d24b6917a54b49de8
Registration Details
Taiwan FDA Registration: 2e301d782cc7248d24b6917a54b49de8
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Device Details

“Schiller” Defibrillators with monitoring functionality
TW: “席樂” 德培克 觸控式生理監視去顫器
Risk Class 3
MD

Registration Details

2e301d782cc7248d24b6917a54b49de8

Ministry of Health Medical Device Import No. 030610

DHA05603061001

Company Information

France

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