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"Aikader" computer-aided diagnostic software - Taiwan Registration dc6887b34e470c2aed7c87bda34c20d0

Access comprehensive regulatory information for "Aikader" 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 dc6887b34e470c2aed7c87bda34c20d0 and manufactured by ICAD INC.. The authorized representative in Taiwan is NAN KAI CORPORATION.

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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dc6887b34e470c2aed7c87bda34c20d0
Registration Details
Taiwan FDA Registration: dc6887b34e470c2aed7c87bda34c20d0
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Device Details

"Aikader" computer-aided diagnostic software
TW: โ€œ่‰พๅกๅพทโ€้›ป่…ฆ่ผ”ๅŠฉ่จบๆ–ท่ปŸ้ซ”
Risk Class 2
Cancelled

Registration Details

dc6887b34e470c2aed7c87bda34c20d0

DHA00602142407

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

Sep 03, 2010

Sep 03, 2015

Jun 08, 2018

Cancellation Information

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