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“SYNTEC” CB-Cervical Cage System - Taiwan Registration bc139d02629e31d011f3baaaa49aad4c

Access comprehensive regulatory information for “SYNTEC” CB-Cervical Cage System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc139d02629e31d011f3baaaa49aad4c and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC 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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bc139d02629e31d011f3baaaa49aad4c
Registration Details
Taiwan FDA Registration: bc139d02629e31d011f3baaaa49aad4c
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Device Details

“SYNTEC” CB-Cervical Cage System
TW: “亞太醫療”亞可-頸椎護架系統
Risk Class 2
MD

Registration Details

bc139d02629e31d011f3baaaa49aad4c

Ministry of Health Medical Device Manufacturing No. 007871

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

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Produced in Taiwan, China

Dates and Status

Jun 07, 2023

Jun 07, 2028