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“Suzuken” Electrocardiograph - Taiwan Registration b1dda91a81fda4a18c87ed4222e92c61

Access comprehensive regulatory information for “Suzuken” Electrocardiograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b1dda91a81fda4a18c87ed4222e92c61 and manufactured by SUZUKEN CO., LTD. The authorized representative in Taiwan is MEDWAY BME CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SUZUKEN CO., LTD, and 1 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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b1dda91a81fda4a18c87ed4222e92c61
Registration Details
Taiwan FDA Registration: b1dda91a81fda4a18c87ed4222e92c61
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Device Details

“Suzuken” Electrocardiograph
TW: “鈴謙” 心電圖描記器
Risk Class 2
MD

Registration Details

b1dda91a81fda4a18c87ed4222e92c61

Ministry of Health Medical Device Import No. 027604

DHA05602760406

Company Information

Japan

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 20, 2015

Aug 20, 2025

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