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“IDOMAN” Thermablate EAS - Taiwan Registration 306014df894899ca707506480abd3142

Access comprehensive regulatory information for “IDOMAN” Thermablate EAS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 306014df894899ca707506480abd3142 and manufactured by Idoman Teoranta. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY 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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306014df894899ca707506480abd3142
Registration Details
Taiwan FDA Registration: 306014df894899ca707506480abd3142
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Device Details

“IDOMAN” Thermablate EAS
TW: “艾多門”子宮內膜消融系統
Risk Class 2
MD

Registration Details

306014df894899ca707506480abd3142

Ministry of Health Medical Device Import No. 031521

DHA05603152104

Company Information

Ireland

Product Details

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

l Devices for obstetrics and gynecology

L9999 Other

Imported from abroad

Dates and Status

Sep 10, 2018

Sep 10, 2023