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"Erip" medical cold compress pack (unsterilized) - Taiwan Registration e94502b2230bbde3ff9d174af8b72a9a

Access comprehensive regulatory information for "Erip" medical cold compress pack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e94502b2230bbde3ff9d174af8b72a9a and manufactured by I-REP Therapy Products, Inc.. The authorized representative in Taiwan is ORTHOHEALTH 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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e94502b2230bbde3ff9d174af8b72a9a
Registration Details
Taiwan FDA Registration: e94502b2230bbde3ff9d174af8b72a9a
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Device Details

"Erip" medical cold compress pack (unsterilized)
TW: "่‰พ็‘žๆ™ฎ"้†ซ็™‚็”จๅ†ทๆ•ทๅŒ…(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e94502b2230bbde3ff9d174af8b72a9a

DHA08401489609

Company Information

United States

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".

o Physical Medical Sciences

O.5700 ้†ซ็™‚็”จๅ†ท็†ฑๆ•ท่ฃ็ฝฎ

import

Dates and Status

Oct 01, 2021

Oct 31, 2025

Nov 21, 2024