"Gelidine" negative pressure wound treatment system - Taiwan Registration b906a54b06eccbf61e45a15c5b066f6c
Access comprehensive regulatory information for "Gelidine" negative pressure wound treatment system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b906a54b06eccbf61e45a15c5b066f6c and manufactured by Genadyne Biotechnology, Inc.. The authorized representative in Taiwan is AMED 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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b906a54b06eccbf61e45a15c5b066f6c
Registration Details
Taiwan FDA Registration: b906a54b06eccbf61e45a15c5b066f6c
Device Details
"Gelidine" negative pressure wound treatment system
TW: โๆฝๅฉๅฎโ่ฒ ๅฃๅทๅฃๆฒป็็ณป็ตฑ
Risk Class 2

