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Keris Polyvinyl Foam Wound Dressing (Sterilized) - Taiwan Registration 54d8a7a2752ca49df0f3802de6e68059

Access comprehensive regulatory information for Keris Polyvinyl 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 54d8a7a2752ca49df0f3802de6e68059 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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54d8a7a2752ca49df0f3802de6e68059
Registration Details
Taiwan FDA Registration: 54d8a7a2752ca49df0f3802de6e68059
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Device Details

Keris Polyvinyl Foam Wound Dressing (Sterilized)
TW: ๅ‡ฑ็‘žๆ–ฏ ่šไน™็ƒฏ้†‡ๆณก็ถฟๅ‚ทๅฃๆ•ทๆ–™ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

54d8a7a2752ca49df0f3802de6e68059

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

Jun 04, 2016

Jun 04, 2021

Aug 28, 2023

Cancellation Information

Logged out

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