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“Schiller” Electrocardiographs - Taiwan Registration 68759066b1b3302e34f980c95d589f72

Access comprehensive regulatory information for “Schiller” Electrocardiographs in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68759066b1b3302e34f980c95d589f72 and manufactured by SCHILLER AG. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SCHILLER AG, and 3 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.

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68759066b1b3302e34f980c95d589f72
Registration Details
Taiwan FDA Registration: 68759066b1b3302e34f980c95d589f72
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Device Details

“Schiller” Electrocardiographs
TW: “錫樂” 心電圖系統
Risk Class 2
MD

Registration Details

68759066b1b3302e34f980c95d589f72

Ministry of Health Medical Device Import No. 028878

DHA05602887809

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E2340 ECG Scanner

Imported from abroad

Dates and Status

Oct 27, 2016

Oct 27, 2026

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