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"Hengyang" cold compress (unsterilized) - Taiwan Registration 20b6b17a0ebcae0b5273af7b85f65d53

Access comprehensive regulatory information for "Hengyang" cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 20b6b17a0ebcae0b5273af7b85f65d53 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is SOLARIS BIOPHARMA 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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20b6b17a0ebcae0b5273af7b85f65d53
Registration Details
Taiwan FDA Registration: 20b6b17a0ebcae0b5273af7b85f65d53
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Device Details

"Hengyang" cold compress (unsterilized)
TW: "ๆ†้™ฝ" ๅ†ทๆ•ท่ฒผ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

20b6b17a0ebcae0b5273af7b85f65d53

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".

o Physical Medical Sciences

O.5700 ้†ซ็™‚็”จๅ†ท็†ฑๆ•ท่ฃ็ฝฎ

Contract manufacturing;; Domestic

Dates and Status

Aug 23, 2016

Aug 23, 2021

Sep 19, 2023

Cancellation Information

Logged out

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