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"Ekia" powered muscle stimulator - Taiwan Registration 557e31e283e42a50acc4f0dfb8d8623f

Access comprehensive regulatory information for "Ekia" powered muscle stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 557e31e283e42a50acc4f0dfb8d8623f 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, 1 companies making similar products including IGEA S.P.A, and 1 recent registrations in the same category. 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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557e31e283e42a50acc4f0dfb8d8623f
Registration Details
Taiwan FDA Registration: 557e31e283e42a50acc4f0dfb8d8623f
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Device Details

"Ekia" powered muscle stimulator
TW: โ€œไปฅๅŸบไบžโ€ๅ‹•ๅŠ›ๅผ่‚Œ่‚‰ๅˆบๆฟ€ๅ™จ
Risk Class 2
Cancelled

Registration Details

557e31e283e42a50acc4f0dfb8d8623f

DHA00602119403

Company Information

Italy

Product Details

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

o Physical Medical Sciences

O.5850 5850.

import

Dates and Status

Jul 07, 2010

Jul 07, 2015

May 21, 2018

Cancellation Information

Logged out

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