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QTM-Dx - Taiwan Registration c881b633ea071f9b828fd4026fb6c513

Access comprehensive regulatory information for QTM-Dx in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c881b633ea071f9b828fd4026fb6c513 and manufactured by QT MEDICAL, INC. TAIWAN BRANCH (U.S.A.). The authorized representative in Taiwan is QT MEDICAL, INC. TAIWAN BRANCH (U.S.A.).

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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c881b633ea071f9b828fd4026fb6c513
Registration Details
Taiwan FDA Registration: c881b633ea071f9b828fd4026fb6c513
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Device Details

QTM-Dx
TW: "ๅฎ‡ๅฟƒ"ๅฟƒ้›ปๅœ–ๅˆ†ๆž่ปŸ้ซ”
Risk Class 2
MD

Registration Details

c881b633ea071f9b828fd4026fb6c513

Ministry of Health Medical Device Manufacturing No. 007312

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E2340 ECG Scanner

Produced in Taiwan, China

Dates and Status

Oct 12, 2021

Oct 12, 2026