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"Rest" titanium sternum fixation system - Taiwan Registration 2d302e4f836d6cec2dc541e972c6f861

Access comprehensive regulatory information for "Rest" titanium sternum 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 2d302e4f836d6cec2dc541e972c6f861 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is Foresee Medical Ltd..

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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2d302e4f836d6cec2dc541e972c6f861
Registration Details
Taiwan FDA Registration: 2d302e4f836d6cec2dc541e972c6f861
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Device Details

"Rest" titanium sternum fixation system
TW: โ€œ่Šฎๆ€็‰นโ€้ˆฆ้‡‘ๅฑฌ่ƒธ้ชจๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

2d302e4f836d6cec2dc541e972c6f861

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N.3030 Single or multiple metallic bone fixation devices and accessories

Contract manufacturing;; Domestic

Dates and Status

Aug 07, 2023

Aug 07, 2028