Taiwan FDA registration b9d7d9259442e5e0acdb638b2a3b1bdc

"Agfa" digital X-ray imaging system

TW: “愛克發”數位X光影像系統
Taiwan flagTaiwan·Risk Class 2·AGFA N.V.·Registered Jul 05, 2013 – Jul 05, 2023Expired
Registration details
Analysis ID
b9d7d9259442e5e0acdb638b2a3b1bdc
Customs Code
DHAS0602499702
Company information
Manufacturer
AGFA N.V.
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
Jul 05, 2013
Expiry Date
Jul 05, 2023
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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 b9d7d9259442e5e0acdb638b2a3b1bdc and manufactured by 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-GEVAERT HEALTHCARE GMBH;; 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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