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"icard" computer-aided diagnostic software - Taiwan Registration f09c4cce2c840ed198e3a0bc22d020a9

Access comprehensive regulatory information for "icard" computer-aided diagnostic software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f09c4cce2c840ed198e3a0bc22d020a9 and manufactured by ICAD INC.. The authorized representative in Taiwan is BEST DIGITAL CO., LTD..

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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f09c4cce2c840ed198e3a0bc22d020a9
Registration Details
Taiwan FDA Registration: f09c4cce2c840ed198e3a0bc22d020a9
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Device Details

"icard" computer-aided diagnostic software
TW: โ€œๆ„›ๅกๅพทโ€้›ป่…ฆ่ผ”ๅŠฉ่จบๆ–ท่ปŸ้ซ”
Risk Class 2
Cancelled

Registration Details

f09c4cce2c840ed198e3a0bc22d020a9

DHA00602189902

Company Information

United States

Product Details

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

P Radiology Science

P.2050 Medical image management and processing systems

import

Dates and Status

Jan 10, 2011

Jan 10, 2021

Oct 06, 2023

Cancellation Information

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