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“Schiller” FRED PA-1 Automated External Defibrillator (AED) - Taiwan Registration 82e19361cae1d3dc976fe4ac0123ff03

Access comprehensive regulatory information for “Schiller” FRED PA-1 Automated External Defibrillator (AED) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 82e19361cae1d3dc976fe4ac0123ff03 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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82e19361cae1d3dc976fe4ac0123ff03
Registration Details
Taiwan FDA Registration: 82e19361cae1d3dc976fe4ac0123ff03
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Device Details

“Schiller” FRED PA-1 Automated External Defibrillator (AED)
TW: “席樂” 費萊德 皮耶萬 自動體外去顫器
Risk Class 3
MD

Registration Details

82e19361cae1d3dc976fe4ac0123ff03

Ministry of Health Medical Device Import No. 030428

DHA05603042809

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

Nov 20, 2017

Nov 20, 2027