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"Agfa" digital X-ray imaging system - Taiwan Registration b9d7d9259442e5e0acdb638b2a3b1bdc

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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b9d7d9259442e5e0acdb638b2a3b1bdc
Registration Details
Taiwan FDA Registration: b9d7d9259442e5e0acdb638b2a3b1bdc
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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

Registration Details

b9d7d9259442e5e0acdb638b2a3b1bdc

DHAS0602499702

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

Jul 05, 2013

Jul 05, 2023