Pure Global

“Durr” compressor (Non-Sterile) - Taiwan Registration ef7d12e10882ca71b16760f907dedec8

Access comprehensive regulatory information for “Durr” compressor (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 ef7d12e10882ca71b16760f907dedec8 and manufactured by DURR DENTAL AG. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
ef7d12e10882ca71b16760f907dedec8
Registration Details
Taiwan FDA Registration: ef7d12e10882ca71b16760f907dedec8
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Durr” compressor (Non-Sterile)
TW: “帝爾” 空氣壓縮機 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

ef7d12e10882ca71b16760f907dedec8

Ministry of Health Medical Device Import No. 014315

DHA09401431501

Company Information

Germany

Product Details

F Dental devices

F6640 Dental Surgical Devices and Their Accessories

Imported from abroad

Dates and Status

Jul 10, 2014

Jul 10, 2019

Jun 07, 2022

Cancellation Information

Logged out

許可證已逾有效期