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“ASTEK” INTERMEDIATE FREQUENCY INTERFERENTIAL CURRENT THERAPY - Taiwan Registration 3a0e9633eded03e8b14b1ddfca1d5172

Access comprehensive regulatory information for “ASTEK” INTERMEDIATE FREQUENCY INTERFERENTIAL CURRENT THERAPY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a0e9633eded03e8b14b1ddfca1d5172 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY 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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3a0e9633eded03e8b14b1ddfca1d5172
Registration Details
Taiwan FDA Registration: 3a0e9633eded03e8b14b1ddfca1d5172
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Device Details

“ASTEK” INTERMEDIATE FREQUENCY INTERFERENTIAL CURRENT THERAPY
TW: “亞星”中頻向量干擾儀
Risk Class 2
MD

Registration Details

3a0e9633eded03e8b14b1ddfca1d5172

Ministry of Health Medical Device Manufacturing No. 004901

Company Information

Taiwan, Province of China

Product Details

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

o Equipment for physical medicine

O5850 powered muscle stimulator

Produced in Taiwan, China

Dates and Status

Mar 05, 2015

Mar 05, 2025