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"Venice" gel cold pack (unsterilized) - Taiwan Registration 4a2f7d5f8b3dbad987f3bbec47931470

Access comprehensive regulatory information for "Venice" gel 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 4a2f7d5f8b3dbad987f3bbec47931470 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES 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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4a2f7d5f8b3dbad987f3bbec47931470
Registration Details
Taiwan FDA Registration: 4a2f7d5f8b3dbad987f3bbec47931470
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Device Details

"Venice" gel cold pack (unsterilized)
TW: "ๅจๅฐผๆ–ฏ"ๅ‡่† ๅ†ทๆ•ทๅŒ…(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

4a2f7d5f8b3dbad987f3bbec47931470

Company Information

Taiwan, Province of China

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

Domestic

Dates and Status

Oct 01, 2021

Oct 31, 2025