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“INTAI” Cannulated Headless Compression Screw System - Taiwan Registration 2de170abbbd51cdd799f8ea90a8eb743

Access comprehensive regulatory information for “INTAI” Cannulated Headless Compression 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 2de170abbbd51cdd799f8ea90a8eb743 and manufactured by Ytterbium Technology Co., Ltd. head office. The authorized representative in Taiwan is Ytterbium Technology Co., Ltd. head office.

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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2de170abbbd51cdd799f8ea90a8eb743
Registration Details
Taiwan FDA Registration: 2de170abbbd51cdd799f8ea90a8eb743
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Device Details

“INTAI” Cannulated Headless Compression Screw System
TW: “鐿鈦”中空無頭加壓釘系統
Risk Class 2
MD

Registration Details

2de170abbbd51cdd799f8ea90a8eb743

Ministry of Health Medical Device Manufacturing No. 007199

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3030 Single or multi-metal bone fixation device and accessories

Produced in Taiwan, China

Dates and Status

Nov 24, 2021

Nov 24, 2026