"Agfa" Developer and Fixer (Non-Sterile)
Taiwan·Risk Class 1·MD·AGFA HEALTHCARE N.V.·Registered Dec 28, 2015 – Dec 28, 2020Cancelled- Analysis ID
- 5ffbaa4157aea093bed84f5a9c13e75b
- License Form
- Ministry of Health Medical Device Import No. 016027
- Customs Code
- DHA09401602703
- Manufacturer
- AGFA HEALTHCARE N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- AGFA MATERIALS TAIWAN CO., LTD.
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1840 Radiographic video
- Import Information
- Imported from abroad
- Registration Date
- Dec 28, 2015
- Expiry Date
- Dec 28, 2020
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 5ffbaa4157aea093bed84f5a9c13e75b and manufactured by AGFA HEALTHCARE 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 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.