Pure Global

“Surgical” Surgiform Augmentation Facial Material - Taiwan Registration a739116820075d3db05ad06e2f05cb69

Access comprehensive regulatory information for “Surgical” Surgiform Augmentation Facial Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a739116820075d3db05ad06e2f05cb69 and manufactured by Surgical Technology Laboratories, Inc.. The authorized representative in Taiwan is J-TRUE MEDICAL INTERNATIONAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
a739116820075d3db05ad06e2f05cb69
Registration Details
Taiwan FDA Registration: a739116820075d3db05ad06e2f05cb69
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Surgical” Surgiform Augmentation Facial Material
TW: “史吉歐”塑吉鋒顏面植入物
Risk Class 2
MD

Registration Details

a739116820075d3db05ad06e2f05cb69

Ministry of Health Medical Device Import No. 030247

DHA05603024705

Company Information

Product Details

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

I General and plastic surgical devices

I3500 Implant material for PTFE containing carbon fiber synthetics

Imported from abroad

Dates and Status

Sep 22, 2017

Sep 22, 2027