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"Cloudcatch" non-aerated hemostatic device (unsterilized) - Taiwan Registration 5e3c8e44a3eeeca7fcae6dd0b5f62641

Access comprehensive regulatory information for "Cloudcatch" non-aerated hemostatic device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5e3c8e44a3eeeca7fcae6dd0b5f62641 and manufactured by TAHAN BIOMEDICAL CO., LTD.. The authorized representative in Taiwan is Yuncai Biotechnology 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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5e3c8e44a3eeeca7fcae6dd0b5f62641
Registration Details
Taiwan FDA Registration: 5e3c8e44a3eeeca7fcae6dd0b5f62641
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Device Details

"Cloudcatch" non-aerated hemostatic device (unsterilized)
TW: "ไบ‘้‡‡" ้žๅ……ๆฐฃๅผๆญข่ก€ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5e3c8e44a3eeeca7fcae6dd0b5f62641

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".

I General, Plastic Surgery and Dermatology

I.5900 ้žๅ……ๆฐฃๅผๆญข่ก€ๅธถ

Domestic;; Contract manufacturing

Dates and Status

Oct 02, 2017

Oct 02, 2022

Apr 12, 2024

Cancellation Information

Logged out

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