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"Ekia" ultrasound therapy device - Taiwan Registration 1ed8359b07aa2c9a97c8756f22466db5

Access comprehensive regulatory information for "Ekia" ultrasound therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1ed8359b07aa2c9a97c8756f22466db5 and manufactured by IGEA S.P.A. The authorized representative in Taiwan is Yajin International Limited.

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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1ed8359b07aa2c9a97c8756f22466db5
Registration Details
Taiwan FDA Registration: 1ed8359b07aa2c9a97c8756f22466db5
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Device Details

"Ekia" ultrasound therapy device
TW: โ€œไปฅๅŸบไบžโ€่ถ…้Ÿณๆณขๆฒป็™‚ๅ„€
Risk Class 3
Cancelled

Registration Details

1ed8359b07aa2c9a97c8756f22466db5

DHA00602051301

Company Information

Italy

Product Details

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

o Physical Medical Sciences

O.5300 ่ถ…้Ÿณๆณข้€็†ฑๆฒป็™‚ๅ„€

import

Dates and Status

Dec 25, 2009

Dec 25, 2014

May 21, 2018

Cancellation Information

Logged out

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