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"Euronda" Saliva Ejector (Non-Sterile) - Taiwan Registration a3d8e68180678606ade30a8a326be537

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..

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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a3d8e68180678606ade30a8a326be537
Registration Details
Taiwan FDA Registration: a3d8e68180678606ade30a8a326be537
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Device Details

"Euronda" Saliva Ejector (Non-Sterile)
TW: "ๅ„ชๆœ—้”" ๅธๅ”พ็ฎก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a3d8e68180678606ade30a8a326be537

Ministry of Health Medical Device Import No. 017384

DHA09401738406

Company Information

Italy

Product Details

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.

F Dental devices

F6640 Dental Surgical Devices and Their Accessories

Imported from abroad

Dates and Status

Jan 09, 2017

Jan 09, 2022