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"Agfa” CEA Radiographic Film (Non-Sterile) - Taiwan Registration bf310baeef6e751e5a11bb7fb1a5e4b0

Access comprehensive regulatory information for "Agfa” CEA Radiographic Film (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 bf310baeef6e751e5a11bb7fb1a5e4b0 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. 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.

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Registration Details
Taiwan FDA Registration: bf310baeef6e751e5a11bb7fb1a5e4b0
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Device Details

"Agfa” CEA Radiographic Film (Non-Sterile)
TW: “愛克發”喜悅醫用X光軟片 (未滅菌)
Risk Class 1
MD

Registration Details

bf310baeef6e751e5a11bb7fb1a5e4b0

Ministry of Health Medical Device Import No. 019760

DHA09401976005

Company Information

Belgium

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