Taiwan FDA registration 55679f25f31dd14f39e61f56bdd13533
“AGFA” Image Processing Software
TW: “愛克發” 影像處理軟體
Taiwan·Risk Class 2·MD·AGFA N.V.·Registered Feb 19, 2014 – Feb 19, 2024ExpiredRegistration details
- Analysis ID
- 55679f25f31dd14f39e61f56bdd13533
- License Form
- Ministry of Health Medical Device Import No. 025818
- Customs Code
- DHA05602581802
Company information
- Manufacturer
- AGFA N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- AGFA MATERIALS TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P2050 Medical Image Management and Processing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 19, 2014
- Expiry Date
- Feb 19, 2024
About this record
Access comprehensive regulatory information for “AGFA” Image Processing Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55679f25f31dd14f39e61f56bdd13533 and manufactured by AGFA N.V.. The authorized representative in Taiwan is AGFA MATERIALS TAIWAN 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.
Free DatabasePowered by Pure Global AI89,000+ Devices