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“BIOPRO”Go-EZ Cannulated Screw System - Taiwan Registration c2f2450207b15b03c96e636ce47da594

Access comprehensive regulatory information for “BIOPRO”Go-EZ Cannulated Screw System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c2f2450207b15b03c96e636ce47da594 and manufactured by BIOPRO, INC.. The authorized representative in Taiwan is EULOGIUMS 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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c2f2450207b15b03c96e636ce47da594
Registration Details
Taiwan FDA Registration: c2f2450207b15b03c96e636ce47da594
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Device Details

“BIOPRO”Go-EZ Cannulated Screw System
TW: “拜歐博”簡易中空骨釘系統
Risk Class 2
MD

Registration Details

c2f2450207b15b03c96e636ce47da594

Ministry of Health Medical Device Import No. 029365

DHA05602936501

Company Information

United States

Product Details

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

N Orthopedic devices

N3040 Smooth or threaded metal bone fixation

Imported from abroad

Dates and Status

Feb 13, 2017

Feb 13, 2027