Taiwan FDA registration 3b94f4dd713ae590f6c4b07bcd095a32
Anker called out
TW: 安克呼止偵
Taiwan·Risk Class 2·AMCAD BIOMED CORPORATION·Registered Nov 05, 2019 – Nov 05, 2029ActiveRegistration details
- Analysis ID
- 3b94f4dd713ae590f6c4b07bcd095a32
Company information
- Manufacturer
- AMCAD BIOMED CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- AMCAD BIOMED CORPORATION
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
- Domestic
Dates and status
- Registration Date
- Nov 05, 2019
- Expiry Date
- Nov 05, 2029
About this record
Access comprehensive regulatory information for Anker called out in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b94f4dd713ae590f6c4b07bcd095a32 and manufactured by AMCAD BIOMED CORPORATION. The authorized representative in Taiwan is AMCAD BIOMED 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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