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"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.

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5ffbaa4157aea093bed84f5a9c13e75b
Registration Details
Taiwan FDA Registration: 5ffbaa4157aea093bed84f5a9c13e75b
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Device Details

"Agfa" Developer and Fixer (Non-Sterile)
TW: "ๆ„›ๅ…‹็™ผ" ้กฏๅฝฑๆถฒ่ˆ‡ๅฎšๅฝฑๆถฒ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

5ffbaa4157aea093bed84f5a9c13e75b

Ministry of Health Medical Device Import No. 016027

DHA09401602703

Company Information

Belgium

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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