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"Agfa" digital X-ray imaging system - Taiwan Registration 61e381f983540e248a5f4b66b7ace5d2

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 61e381f983540e248a5f4b66b7ace5d2 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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61e381f983540e248a5f4b66b7ace5d2
Registration Details
Taiwan FDA Registration: 61e381f983540e248a5f4b66b7ace5d2
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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

61e381f983540e248a5f4b66b7ace5d2

DHA05602877601

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

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

Dates and Status

Sep 01, 2016

Sep 01, 2021

Sep 23, 2023

Cancellation Information

Logged out

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