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"Kanglidu" Hengmei Scar Patch (Unsterilized) - Taiwan Registration 4ed5480cbba6268fddbd8ceb648498c3

Access comprehensive regulatory information for "Kanglidu" Hengmei Scar Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ed5480cbba6268fddbd8ceb648498c3 and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is CORELEADER BIOTECH 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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4ed5480cbba6268fddbd8ceb648498c3
Registration Details
Taiwan FDA Registration: 4ed5480cbba6268fddbd8ceb648498c3
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Device Details

"Kanglidu" Hengmei Scar Patch (Unsterilized)
TW: "ๅบทๅŠ›ๅพ—" ๆ†็พŽ็–ค็—•่ฒผ็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4ed5480cbba6268fddbd8ceb648498c3

Company Information

Product Details

Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".

I General, Plastic Surgery and Dermatology

I.4025 Silicone products for scar treatment

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Dates and Status

Oct 16, 2015

Oct 16, 2020

Jun 22, 2022

Cancellation Information

Logged out

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