Taiwan FDA registration e46a1e9c938073f332dfc221905c65ee
“CEFLA” RX DC Intraoral Source X-Ray System
TW: “錫夫拉”口腔內X光照射系統
Taiwan·Risk Class 2·MD·Cefla S.C.;;CEFLA S.C.·Registered Sep 14, 2023 – Sep 14, 2028ActiveRegistration details
- Analysis ID
- e46a1e9c938073f332dfc221905c65ee
- License Form
- Ministry of Health Medical Device Import No. 036730
- Customs Code
- DHAS5603673007
Company information
- Manufacturer
- Cefla S.C.;;CEFLA S.C.
- Manufacturer Country
- Italy
- Authorized Representative
- KAO TECH MD CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F1800 Extraoral X-ray System
- Import Information
- 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
- Registration Date
- Sep 14, 2023
- Expiry Date
- Sep 14, 2028
About this record
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..
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