Taiwan FDA registration 90727d1225bd0b12dd18c44a6ed34950

"Agfa" digital X-ray imaging system

TW: “愛克發” 數位X光影像系統
Taiwan flagTaiwan·Risk Class 2·AGFA HEALTHCARE N. V.·Registered Jun 13, 2014 – Jun 13, 2019Cancelled
Registration details
Analysis ID
90727d1225bd0b12dd18c44a6ed34950
Customs Code
DHAS5602624609
Company information
Manufacturer Country
Belgium
Authorized Representative
AGFA MATERIALS TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1680 固定式X光系統
Import Information
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Jun 13, 2014
Expiry Date
Jun 13, 2019
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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