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"Agfa" dry printing machine - Taiwan Registration f945542d859708cadf7a6bc864921ccd

Access comprehensive regulatory information for "Agfa" dry printing machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f945542d859708cadf7a6bc864921ccd and manufactured by AGFA-GEVAERT HEALTHCARE GMBH;; 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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f945542d859708cadf7a6bc864921ccd
Registration Details
Taiwan FDA Registration: f945542d859708cadf7a6bc864921ccd
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Device Details

"Agfa" dry printing machine
TW: "ๆ„›ๅ…‹็™ผ" ไนพๅผๅฐ็‰‡ๆฉŸ
Risk Class 2

Registration Details

f945542d859708cadf7a6bc864921ccd

DHA00601265907

Company Information

Belgium;;Germany

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

import

Dates and Status

Oct 12, 2005

Oct 12, 2025