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"Kinetec" Water circulating hot or cold pack (Non-Sterile) - Taiwan Registration 6c294bc9147529209b4ce18c570d03aa

Access comprehensive regulatory information for "Kinetec" 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 6c294bc9147529209b4ce18c570d03aa and manufactured by KINETEC SAS. The authorized representative in Taiwan is BLESSING CATHAY 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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6c294bc9147529209b4ce18c570d03aa
Registration Details
Taiwan FDA Registration: 6c294bc9147529209b4ce18c570d03aa
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Device Details

"Kinetec" Water circulating hot or cold pack (Non-Sterile)
TW: "่‚ฏๅฐผๅธๅ…‹" ้†ซ็™‚็”จๆฐดๅพช็’ฐๅผๅ†ท็†ฑๆ•ทๅŒ… (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6c294bc9147529209b4ce18c570d03aa

Ministry of Health Medical Device Import No. 016283

DHA09401628308

Company Information

France

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

Imported from abroad

Dates and Status

Mar 21, 2016

Mar 21, 2021