Taiwan FDA registration a3d8e68180678606ade30a8a326be537
"Euronda" Saliva Ejector (Non-Sterile)
TW: "優朗達" 吸唾管 (未滅菌)
Taiwan·Risk Class 1·MD·EURONDA SPA·Registered Jan 09, 2017 – Jan 09, 2022ExpiredRegistration details
- Analysis ID
- a3d8e68180678606ade30a8a326be537
- License Form
- Ministry of Health Medical Device Import No. 017384
- Customs Code
- DHA09401738406
Company information
- Manufacturer
- EURONDA SPA
- Manufacturer Country
- Italy
- Authorized Representative
- FABRO INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6640 Dental Surgical Devices and Their Accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 09, 2017
- Expiry Date
- Jan 09, 2022
About this record
Access comprehensive regulatory information for "Euronda" Saliva Ejector (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 a3d8e68180678606ade30a8a326be537 and manufactured by EURONDA SPA. The authorized representative in Taiwan is FABRO INTERNATIONAL CO., LTD..
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