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“LUMARK” Water circulating hot or cold pack (Non-sterile) - Taiwan Registration 5ec2281d6f0c5b771c14a0121dd989af

Access comprehensive regulatory information for “LUMARK” Water circulating hot or cold pack (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 5ec2281d6f0c5b771c14a0121dd989af and manufactured by Luma Enterprises Limited New House Factory. The authorized representative in Taiwan is LU MARK ENTERPRISES INC..

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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5ec2281d6f0c5b771c14a0121dd989af
Registration Details
Taiwan FDA Registration: 5ec2281d6f0c5b771c14a0121dd989af
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Device Details

“LUMARK” Water circulating hot or cold pack (Non-sterile)
TW: “璐瑪”醫療用水循環式冷熱敷包(未滅菌)
Risk Class 1
MD

Registration Details

5ec2281d6f0c5b771c14a0121dd989af

Ministry of Health Medical Device Manufacturing No. 008598

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Medical Water Recycling Hot and Cold Compress Pack (O.5720)".

o Equipment for physical medicine

O5720 Medical Water Recycling Hot and Cold Pack

Produced in Taiwan, China

Dates and Status

Sep 11, 2020

Sep 11, 2025