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“Koelis” TRINITY - Taiwan Registration bbbb4fc54ec23fa0c66ba9fedf622d19

Access comprehensive regulatory information for “Koelis” TRINITY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bbbb4fc54ec23fa0c66ba9fedf622d19 and manufactured by KOELIS. The authorized representative in Taiwan is TAIWAN MEDICAL SUPPLY, INC..

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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bbbb4fc54ec23fa0c66ba9fedf622d19
Registration Details
Taiwan FDA Registration: bbbb4fc54ec23fa0c66ba9fedf622d19
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Device Details

“Koelis” TRINITY
TW: “可立”超音波系統及其附件
Risk Class 2
MD

Registration Details

bbbb4fc54ec23fa0c66ba9fedf622d19

Ministry of Health Medical Device Import No. 032603

DHA05603260301

Company Information

France

Product Details

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

P Devices for radiology

P1560 ultrasonic echo imaging system

Imported from abroad

Dates and Status

May 08, 2019

May 08, 2024