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"Spectrum" Spectragel 2Q (non-sterile) - Taiwan Registration 58bf0275fcac8d8343b1afb268d7d89f

Access comprehensive regulatory information for "Spectrum" Spectragel 2Q (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 58bf0275fcac8d8343b1afb268d7d89f and manufactured by SPECTRUM DESIGNS, INC.. The authorized representative in Taiwan is Beleli Biotechnology 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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58bf0275fcac8d8343b1afb268d7d89f
Registration Details
Taiwan FDA Registration: 58bf0275fcac8d8343b1afb268d7d89f
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Device Details

"Spectrum" Spectragel 2Q (non-sterile)
TW: "ๆ€่ฒๅผท" ็–ค็—•ๅ‡่†  (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

58bf0275fcac8d8343b1afb268d7d89f

Ministry of Health Medical Device Import No. 015028

DHA09401502800

Company Information

United States

Product Details

I General and plastic surgical devices

I4025 Scar Treatment Silicone Products

Imported from abroad

Dates and Status

Mar 23, 2015

Mar 23, 2020

Jun 22, 2022

Cancellation Information

Logged out

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