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“Sciton” BBLs System - Taiwan Registration 3c7b5bf796f978e4e2f20ebe1b56959b

Access comprehensive regulatory information for “Sciton” BBLs System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3c7b5bf796f978e4e2f20ebe1b56959b and manufactured by SCITON, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL 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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3c7b5bf796f978e4e2f20ebe1b56959b
Registration Details
Taiwan FDA Registration: 3c7b5bf796f978e4e2f20ebe1b56959b
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Device Details

“Sciton” BBLs System
TW: “賽頓”吉爾寬頻光照系統
Risk Class 2
MD
Cancelled

Registration Details

3c7b5bf796f978e4e2f20ebe1b56959b

Ministry of Health Medical Device Import No. 027133

DHA05602713306

Company Information

United States

Product Details

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Mar 12, 2015

Mar 12, 2020

Jun 16, 2022

Cancellation Information

Logged out

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