Taiwan FDA registration 2de170abbbd51cdd799f8ea90a8eb743

“INTAI” Cannulated Headless Compression Screw System

TW: “鐿鈦”中空無頭加壓釘系統

Taiwan·Risk Class 2·MD·Ytterbium Technology Co., Ltd. head office·Registered Nov 24, 2021 – Nov 24, 2026Active

Registration details

Analysis ID: 2de170abbbd51cdd799f8ea90a8eb743
License Form: Ministry of Health Medical Device Manufacturing No. 007199

Company information

Manufacturer: Ytterbium Technology Co., Ltd. head office
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Ytterbium Technology Co., Ltd. head office

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N3030 Single or multi-metal bone fixation device and accessories
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Nov 24, 2021
Expiry Date: Nov 24, 2026

About this record

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.

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