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“AGFA”Dentus Film(Non-Sterile) - Taiwan Registration 521cb543c08f431f936d895cd144e5a5

Access comprehensive regulatory information for “AGFA”Dentus Film(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 521cb543c08f431f936d895cd144e5a5 and manufactured by AGFA HEALTHCARE N. V.. The authorized representative in Taiwan is ANDLIFE INC..

This page provides complete technical specifications, regulatory compliance details. 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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521cb543c08f431f936d895cd144e5a5
Registration Details
Taiwan FDA Registration: 521cb543c08f431f936d895cd144e5a5
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Device Details

“AGFA”Dentus Film(Non-Sterile)
TW: “艾克發”牙科用X-光軟片(未滅菌)
Risk Class 1
MD

Registration Details

521cb543c08f431f936d895cd144e5a5

Ministry of Health Medical Device Import No. 013700

DHA09401370009

Company Information

Belgium

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".

P Devices for radiology

P1840 Radiographic video

Imported from abroad

Dates and Status

Dec 20, 2013

Dec 20, 2023