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“Neodyne”Silicone Scar-care Dressing (Non-Sterile) - Taiwan Registration a1839e7c9074adf85243a89e3f7b550f

Access comprehensive regulatory information for “Neodyne”Silicone Scar-care Dressing (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a1839e7c9074adf85243a89e3f7b550f and manufactured by NEODYNE BIOSCIENCES, INC.. The authorized representative in Taiwan is Robbie Jenny International Inc.

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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a1839e7c9074adf85243a89e3f7b550f
Registration Details
Taiwan FDA Registration: a1839e7c9074adf85243a89e3f7b550f
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Device Details

“Neodyne”Silicone Scar-care Dressing (Non-Sterile)
TW: “尼德”疤痕護理矽膠片 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

a1839e7c9074adf85243a89e3f7b550f

Ministry of Health Medical Device Import No. 013735

DHA09401373502

Company Information

United States

Product Details

I General and plastic surgical devices

I4025 silicone sheet

Imported from abroad

Dates and Status

Dec 27, 2013

Dec 27, 2018

Feb 11, 2019

Cancellation Information

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