"Agfa" Developer and Fixer (Non-Sterile) - Taiwan Registration 5ffbaa4157aea093bed84f5a9c13e75b
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.
Device Details
Registration Details
5ffbaa4157aea093bed84f5a9c13e75b
Ministry of Health Medical Device Import No. 016027
DHA09401602703
Product Details
P Devices for radiology
P1840 Radiographic video
Imported from abroad
Dates and Status
Dec 28, 2015
Dec 28, 2020
Aug 05, 2022
Cancellation Information
Logged out
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