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"Kangis Mei" hot and cold compress pad (unsterilized) - Taiwan Registration dc8924bb1f6feb0c9b218b339d67cc3c

Access comprehensive regulatory information for "Kangis Mei" hot and cold compress pad (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dc8924bb1f6feb0c9b218b339d67cc3c and manufactured by Laili Enterprises Co., Ltd. The authorized representative in Taiwan is PRESIDENT DRUGSTORE BUSINESS CORPORATION.

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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dc8924bb1f6feb0c9b218b339d67cc3c
Registration Details
Taiwan FDA Registration: dc8924bb1f6feb0c9b218b339d67cc3c
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Device Details

"Kangis Mei" hot and cold compress pad (unsterilized)
TW: โ€œๅบทๆ˜ฏ็พŽโ€ๅ†ท็†ฑๆ•ทๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dc8924bb1f6feb0c9b218b339d67cc3c

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".

o Physical Medical Sciences

O.5710 ้†ซ็™‚็”จๅฏไธŸๆฃ„ๅผ็š„ๅ†ท็†ฑๆ•ทๅŒ…

Domestic;; Contract manufacturing

Dates and Status

May 11, 2012

May 11, 2017

Dec 13, 2019

Cancellation Information

Logged out

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