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“Schiller” Electrocardiographs - Taiwan Registration a2648c27eb4b35f94b793111639c3776

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 a2648c27eb4b35f94b793111639c3776 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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a2648c27eb4b35f94b793111639c3776
Registration Details
Taiwan FDA Registration: a2648c27eb4b35f94b793111639c3776
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Device Details

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

Registration Details

a2648c27eb4b35f94b793111639c3776

Ministry of Health Medical Device Import No. 026434

DHA05602643402

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

Aug 14, 2014

Aug 14, 2024

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