"Agfa" Developer and Fixer (Non-Sterile)
Taiwan·Risk Class 1·MD·AGFA N.V.·Registered Nov 01, 2018 – Nov 01, 2028Active- Analysis ID
- 54dba9f246302cebb069a93ae2b4894f
- License Form
- Ministry of Health Medical Device Import No. 019761
- Customs Code
- DHA09401976107
- Manufacturer
- AGFA N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- AGFA MATERIALS TAIWAN CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1840 Radiographic video
- Import Information
- Imported from abroad
- Registration Date
- Nov 01, 2018
- Expiry Date
- Nov 01, 2028
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Access comprehensive regulatory information for "Agfa" Developer and Fixer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 54dba9f246302cebb069a93ae2b4894f 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, 1 companies making similar products including AGFA HEALTHCARE N.V., and 1 recent registrations in the same category. 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.