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“BIOPLATE” Preformed Fixation System - Taiwan Registration 504a5890eafa967b4cbca04e1b34fa2a

Access comprehensive regulatory information for “BIOPLATE” Preformed Fixation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 504a5890eafa967b4cbca04e1b34fa2a and manufactured by BIOPLATE, INC.. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.

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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504a5890eafa967b4cbca04e1b34fa2a
Registration Details
Taiwan FDA Registration: 504a5890eafa967b4cbca04e1b34fa2a
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Device Details

“BIOPLATE” Preformed Fixation System
TW: “拜普雷”預成形固定系統
Risk Class 2
MD

Registration Details

504a5890eafa967b4cbca04e1b34fa2a

Ministry of Health Medical Device Import No. 028985

DHA05602898500

Company Information

United States

Product Details

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

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Imported from abroad

Dates and Status

Oct 17, 2016

Oct 17, 2026