"Agfa" Developer and Fixer (Non-Sterile) - Taiwan Registration 54dba9f246302cebb069a93ae2b4894f
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.
Device Details
Registration Details
54dba9f246302cebb069a93ae2b4894f
Ministry of Health Medical Device Import No. 019761
DHA09401976107
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".
P Devices for radiology
P1840 Radiographic video
Imported from abroad
Dates and Status
Nov 01, 2018
Nov 01, 2028