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“CEFLA” RX DC Intraoral Source X-Ray System - Taiwan Registration e46a1e9c938073f332dfc221905c65ee

Access comprehensive regulatory information for “CEFLA” RX DC Intraoral Source X-Ray System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e46a1e9c938073f332dfc221905c65ee and manufactured by Cefla S.C.;;CEFLA S.C.. The authorized representative in Taiwan is KAO TECH MD CO., LTD..

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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e46a1e9c938073f332dfc221905c65ee
Registration Details
Taiwan FDA Registration: e46a1e9c938073f332dfc221905c65ee
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Device Details

“CEFLA” RX DC Intraoral Source X-Ray System
TW: “錫夫拉”口腔內X光照射系統
Risk Class 2
MD

Registration Details

e46a1e9c938073f332dfc221905c65ee

Ministry of Health Medical Device Import No. 036730

DHAS5603673007

Company Information

Italy

Product Details

Details are as detailed as approved Chinese instructions

F Dentistry

F1800 Extraoral X-ray System

Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)

Dates and Status

Sep 14, 2023

Sep 14, 2028