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“funcare” Pulse Therapy Unit - Taiwan Registration 79ef404da4eb25e9590ec63803b2a27c

Access comprehensive regulatory information for “funcare” Pulse Therapy Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79ef404da4eb25e9590ec63803b2a27c 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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79ef404da4eb25e9590ec63803b2a27c
Registration Details
Taiwan FDA Registration: 79ef404da4eb25e9590ec63803b2a27c
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Device Details

“funcare” Pulse Therapy Unit
TW: “船井”脈衝儀
Risk Class 2
MD

Registration Details

79ef404da4eb25e9590ec63803b2a27c

Ministry of Health Medical Device Manufacturing No. 005239

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

Dec 24, 2015

Dec 24, 2025