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"Fentith" hot and cold compress (unsterilized) - Taiwan Registration 4fea071a71eba07eca4656beb23b9ffe

Access comprehensive regulatory information for "Fentith" hot and 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 4fea071a71eba07eca4656beb23b9ffe and manufactured by Hongxing Plastic Co., Ltd. Zhonghe Factory. The authorized representative in Taiwan is FANTASY INDUSTRY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Fendis Industries Limited;; Hongxing Plastic Co., Ltd. neutralization plant, and 1 recent registrations in the same category. 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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4fea071a71eba07eca4656beb23b9ffe
Registration Details
Taiwan FDA Registration: 4fea071a71eba07eca4656beb23b9ffe
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Device Details

"Fentith" hot and cold compress (unsterilized)
TW: โ€œ่Šฌ่’‚ๆ€โ€ๅ†ท็†ฑๆ•ทๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4fea071a71eba07eca4656beb23b9ffe

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

Domestic;; Contract manufacturing

Dates and Status

Nov 27, 2007

Nov 27, 2022

Sep 30, 2021

Cancellation Information

Logged out

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