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"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
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Device Details

"Gelidine" negative pressure wound treatment system
TW: โ€œๆฝ”ๅˆฉๅฎšโ€่ฒ ๅฃ“ๅ‚ทๅฃๆฒป็™‚็ณป็ตฑ
Risk Class 2

Registration Details

b906a54b06eccbf61e45a15c5b066f6c

DHA05602750201

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.4780 ๅ‹•ๅŠ›ๅผๆŠฝๅธๅนซๆตฆ

import

Dates and Status

Jul 17, 2015

Jul 17, 2025