Taiwan FDA registration f945542d859708cadf7a6bc864921ccd
"Agfa" dry printing machine
TW: "愛克發" 乾式印片機
Taiwan·Risk Class 2·AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.·Registered Oct 12, 2005 – Oct 12, 2025ExpiredRegistration details
- Analysis ID
- f945542d859708cadf7a6bc864921ccd
- Customs Code
- DHA00601265907
Company information
- Manufacturer
- AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.
- Manufacturer Country
- Belgium;;Germany
- 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 Radiology Science
- Import Information
- import
Dates and status
- Registration Date
- Oct 12, 2005
- Expiry Date
- Oct 12, 2025
About this record
Access comprehensive regulatory information for "Agfa" dry printing machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f945542d859708cadf7a6bc864921ccd and manufactured by AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.. The authorized representative in Taiwan is AGFA MATERIALS TAIWAN CO., LTD..
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