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"Agfa" digital X-ray imaging system - Taiwan Registration 90727d1225bd0b12dd18c44a6ed34950

Access comprehensive regulatory information for "Agfa" digital X-ray imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 90727d1225bd0b12dd18c44a6ed34950 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, 2 companies making similar products including AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V., AGFA N.V., and 4 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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90727d1225bd0b12dd18c44a6ed34950
Registration Details
Taiwan FDA Registration: 90727d1225bd0b12dd18c44a6ed34950
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Device Details

"Agfa" digital X-ray imaging system
TW: โ€œๆ„›ๅ…‹็™ผโ€ ๆ•ธไฝXๅ…‰ๅฝฑๅƒ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

90727d1225bd0b12dd18c44a6ed34950

DHAS5602624609

Company Information

Belgium

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jun 13, 2014

Jun 13, 2019

Aug 05, 2022

Cancellation Information

Logged out

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