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"Keris" foam wound dressing (sterilized) - Taiwan Registration 26c4762a0f3fa7c5d6558d77b5501213

Access comprehensive regulatory information for "Keris" foam wound dressing (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 26c4762a0f3fa7c5d6558d77b5501213 and manufactured by SHI HENG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHI HENG TECHNOLOGY 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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26c4762a0f3fa7c5d6558d77b5501213
Registration Details
Taiwan FDA Registration: 26c4762a0f3fa7c5d6558d77b5501213
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Device Details

"Keris" foam wound dressing (sterilized)
TW: "ๅ‡ฑ็‘žๆ–ฏ" ๆณก็ถฟๅ‚ทๅฃๆ•ทๆ–™ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

26c4762a0f3fa7c5d6558d77b5501213

Company Information

Taiwan, Province of China

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".

I General, Plastic Surgery and Dermatology

I.4018 ่ฆชๆฐดๆ€งๅ‰ตๅ‚ท่ฆ†่“‹ๆ

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Dec 29, 2016

Dec 29, 2021

Aug 28, 2023

Cancellation Information

Logged out

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