Taiwan FDA registration f09c4cce2c840ed198e3a0bc22d020a9
"icard" computer-aided diagnostic software
TW: “愛卡德”電腦輔助診斷軟體
Registration details
- Analysis ID
- f09c4cce2c840ed198e3a0bc22d020a9
- Customs Code
- DHA00602189902
Company information
- Manufacturer
- ICAD INC.
- Manufacturer Country
- United States
- Authorized Representative
- BEST DIGITAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.2050 Medical image management and processing systems
- Import Information
- import
Dates and status
- Registration Date
- Jan 10, 2011
- Expiry Date
- Jan 10, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
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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