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“OMNIPORE” Surgical Implants - Taiwan Registration 23179d8dafe7f82085a519506f052d1f

Access comprehensive regulatory information for “OMNIPORE” Surgical Implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 23179d8dafe7f82085a519506f052d1f and manufactured by MATRIX SURGICAL HOLDINGS, LLC. 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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23179d8dafe7f82085a519506f052d1f
Registration Details
Taiwan FDA Registration: 23179d8dafe7f82085a519506f052d1f
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Device Details

“OMNIPORE” Surgical Implants
TW: "傲密補" 植入式人工骨
Risk Class 2
MD

Registration Details

23179d8dafe7f82085a519506f052d1f

Ministry of Health Medical Device Import No. 028374

DHA05602837407

Company Information

United States

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

Apr 14, 2016

Apr 14, 2026