Taiwan FDA registration 557e31e283e42a50acc4f0dfb8d8623f

"Ekia" powered muscle stimulator

TW: “以基亞”動力式肌肉刺激器
Taiwan flagTaiwan·Risk Class 2·IGEA S.P.A·Registered Jul 07, 2010 – Jul 07, 2015Cancelled
Registration details
Analysis ID
557e31e283e42a50acc4f0dfb8d8623f
Customs Code
DHA00602119403
Company information
Manufacturer
IGEA S.P.A
Manufacturer Country
Italy
Authorized Representative
Yajin International Limited
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.5850 5850.
Import Information
import
Dates and status
Registration Date
Jul 07, 2010
Expiry Date
Jul 07, 2015
Cancellation Date
May 21, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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