Taiwan FDA registration a51db83ee6662ae53b099b0e238eb59d
Anker Detective
TW: 安克甲狀偵
Taiwan·Risk Class 2·AMCAD BIOMED CORPORATION·Registered Jan 22, 2015 – Jan 22, 2030ActiveRegistration details
- Analysis ID
- a51db83ee6662ae53b099b0e238eb59d
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. Increased efficiency, as detailed in the Chinese approved copy of the replica (the original approved copy of the Chinese on 3 February 104 is withdrawn and invalidated).
- 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
- Jan 22, 2015
- Expiry Date
- Jan 22, 2030
About this record
Access comprehensive regulatory information for Anker Detective in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a51db83ee6662ae53b099b0e238eb59d 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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