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“Mego Afek” compression therapy systems - Taiwan Registration b0809d9fbeb1e781ebf1a5455b2763ef

Access comprehensive regulatory information for “Mego Afek” compression therapy systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0809d9fbeb1e781ebf1a5455b2763ef and manufactured by MEGO AFEK ACS LTD.. The authorized representative in Taiwan is Yuanhong Instrument Co., 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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b0809d9fbeb1e781ebf1a5455b2763ef
Registration Details
Taiwan FDA Registration: b0809d9fbeb1e781ebf1a5455b2763ef
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Device Details

“Mego Afek” compression therapy systems
TW: “美固雅飛克”氣壓治療系統
Risk Class 2
MD

Registration Details

b0809d9fbeb1e781ebf1a5455b2763ef

Ministry of Health Medical Device Import No. 032606

DHA05603260604

Company Information

Israel

Product Details

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

o Equipment for physical medicine

O5650 Power Expansion Tubular Massager

Imported from abroad

Dates and Status

May 13, 2019

May 13, 2024