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“E.M.S.” AIR-FLOW MASTER - Taiwan Registration 3f5a77858f3d75ab721d12f06d5a5450

Access comprehensive regulatory information for “E.M.S.” AIR-FLOW MASTER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f5a77858f3d75ab721d12f06d5a5450 and manufactured by E.M.S. Electro Medical Systems S.A.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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3f5a77858f3d75ab721d12f06d5a5450
Registration Details
Taiwan FDA Registration: 3f5a77858f3d75ab721d12f06d5a5450
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Device Details

“E.M.S.” AIR-FLOW MASTER
TW: “伊雷卓醫療系統”超音波噴砂潔牙機
Risk Class 2
MD

Registration Details

3f5a77858f3d75ab721d12f06d5a5450

Ministry of Health Medical Device Import No. 028830

DHA05602883007

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F4850 ultrasonic dental cleanser

Imported from abroad

Dates and Status

Sep 12, 2016

Sep 12, 2026