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“SYNTEC” Occipital-Cervical-Upper Thoracic Fixation System - Taiwan Registration 5f09780e00cb0c7766c9c3d24bff3900

Access comprehensive regulatory information for “SYNTEC” Occipital-Cervical-Upper Thoracic 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 5f09780e00cb0c7766c9c3d24bff3900 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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5f09780e00cb0c7766c9c3d24bff3900
Registration Details
Taiwan FDA Registration: 5f09780e00cb0c7766c9c3d24bff3900
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Device Details

“SYNTEC” Occipital-Cervical-Upper Thoracic Fixation System
TW: “亞太醫療”龍頸柱系統
Risk Class 2
MD

Registration Details

5f09780e00cb0c7766c9c3d24bff3900

Ministry of Health Medical Device Manufacturing No. 007380

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3075 Posterior cervical peduncle screw system

Produced in Taiwan, China

Dates and Status

Apr 20, 2022

Apr 20, 2027