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AIRIP Medical Cold Pack (Unsterilized) - Taiwan Registration af64707a621bc63389c5738ecab4ddac

Access comprehensive regulatory information for AIRIP Medical Cold 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 af64707a621bc63389c5738ecab4ddac and manufactured by I-REP Therapy Products, Inc.. The authorized representative in Taiwan is TISSUKINE 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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af64707a621bc63389c5738ecab4ddac
Registration Details
Taiwan FDA Registration: af64707a621bc63389c5738ecab4ddac
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Device Details

AIRIP Medical Cold Pack (Unsterilized)
TW: ่‰พ้Šณๆ™ฎ ้†ซ็™‚็”จๅ†ทๆ•ทๅŒ… (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

af64707a621bc63389c5738ecab4ddac

DHA084a0010501

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

Dates and Status

Sep 02, 2022

Oct 31, 2025