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"Joy" developer and fixer (unsterilized) - Taiwan Registration cc879cd80d925cd1aa97884060e93f12

Access comprehensive regulatory information for "Joy" developer and fixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cc879cd80d925cd1aa97884060e93f12 and manufactured by AGFA HEALTHCARE N. V.. The authorized representative in Taiwan is Taiwan Agfa Medical Equipment 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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cc879cd80d925cd1aa97884060e93f12
Registration Details
Taiwan FDA Registration: cc879cd80d925cd1aa97884060e93f12
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Device Details

"Joy" developer and fixer (unsterilized)
TW: "ๅ–œๆ‚…"้กฏๅฝฑๆถฒ่ˆ‡ๅฎšๅฝฑๆถฒ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

cc879cd80d925cd1aa97884060e93f12

DHA04400290000

Company Information

Belgium

Product Details

Liquids for the processing of radiographic films.

P Radiology Science

P.1840 Radiographic film

import

Dates and Status

Mar 13, 2006

Mar 13, 2016

Apr 25, 2018

Cancellation Information

Logged out

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