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"Agfa" digital X-ray imaging system - Taiwan Registration 6336f8a8985a95155ecb1eb458e576c4

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 6336f8a8985a95155ecb1eb458e576c4 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, 3 companies making similar products including AGFA N.V., AGFA HEALTHCARE 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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6336f8a8985a95155ecb1eb458e576c4
Registration Details
Taiwan FDA Registration: 6336f8a8985a95155ecb1eb458e576c4
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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

6336f8a8985a95155ecb1eb458e576c4

DHAS5603041702

Company Information

Belgium;;Germany

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Nov 13, 2017

Nov 13, 2022

Apr 12, 2024

Cancellation Information

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