Pure Global

“SYNTEC” Cannulated Screw System - Taiwan Registration 9e0f1a0975e6a1a32062a2db099508c3

Access comprehensive regulatory information for “SYNTEC” 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 9e0f1a0975e6a1a32062a2db099508c3 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
9e0f1a0975e6a1a32062a2db099508c3
Registration Details
Taiwan FDA Registration: 9e0f1a0975e6a1a32062a2db099508c3
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“SYNTEC” Cannulated Screw System
TW: “亞太醫療”中空骨釘系統
Risk Class 2
MD

Registration Details

9e0f1a0975e6a1a32062a2db099508c3

Ministry of Health Medical Device Manufacturing No. 007355

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3040 Smooth or threaded metal bone fixation

Produced in Taiwan, China

Dates and Status

Dec 31, 2021

Dec 31, 2026