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"Fentith" hot and cold compress (unsterilized) - Taiwan Registration 8f6484e647dfdc101eda3c942f903e82

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 8f6484e647dfdc101eda3c942f903e82 and manufactured by Fendis Industries Limited;; Hongxing Plastic Co., Ltd. neutralization plant. 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 Hongxing Plastic Co., Ltd. Zhonghe Factory, 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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8f6484e647dfdc101eda3c942f903e82
Registration Details
Taiwan FDA Registration: 8f6484e647dfdc101eda3c942f903e82
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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

8f6484e647dfdc101eda3c942f903e82

Company Information

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;; Contract manufacturing

Dates and Status

Oct 01, 2021

Oct 31, 2023

Nov 02, 2023

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€…

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