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REXICARE AIR ACTIVATED HEAT PATCH (Non-sterile) - Taiwan Registration 4cc777bb4fb2e2430f3ca585aa310cdd

Access comprehensive regulatory information for REXICARE AIR ACTIVATED HEAT PATCH (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4cc777bb4fb2e2430f3ca585aa310cdd and manufactured by R&R MEDICAL CORPORATION LTD.. The authorized representative in Taiwan is R&R MEDICAL CORPORATION 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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4cc777bb4fb2e2430f3ca585aa310cdd
Registration Details
Taiwan FDA Registration: 4cc777bb4fb2e2430f3ca585aa310cdd
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Device Details

REXICARE AIR ACTIVATED HEAT PATCH (Non-sterile)
TW: ็‘žๆ–ฏ ๆบซ็†ฑๆ•ท่ฒผ็‰‡(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4cc777bb4fb2e2430f3ca585aa310cdd

Ministry of Health Medical Device Manufacturing No. 007109

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".

o Equipment for physical medicine

O5710 Discardable Hot and Cold Compress for Medical Use

Produced in Taiwan, China

Dates and Status

Feb 09, 2018

Feb 09, 2023