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"Retik" electrotherapy device - Taiwan Registration 055717bd61c84d3a1243c06b8e857bcb

Access comprehensive regulatory information for "Retik" electrotherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 055717bd61c84d3a1243c06b8e857bcb and manufactured by RELTEC Medical Devices Corporation. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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055717bd61c84d3a1243c06b8e857bcb
Registration Details
Taiwan FDA Registration: 055717bd61c84d3a1243c06b8e857bcb
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Device Details

"Retik" electrotherapy device
TW: โ€œ้›ท่’‚ๅ…‹โ€ ้›ปไฝๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

055717bd61c84d3a1243c06b8e857bcb

DHA05603728700

Company Information

Product Details

Details are as detailed as approved Chinese instructions

o Physical Medical Sciences

O.0001 ้œ้›ปๅ™จ(้›ปไฝๆฒป็™‚ๅ™จ)

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Dates and Status

Aug 18, 2024

Aug 18, 2029