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"Rest" funnel chest correction system - Taiwan Registration ae39fefe6d01392ada1a2243c3ac234a

Access comprehensive regulatory information for "Rest" funnel chest correction system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae39fefe6d01392ada1a2243c3ac234a 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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ae39fefe6d01392ada1a2243c3ac234a
Registration Details
Taiwan FDA Registration: ae39fefe6d01392ada1a2243c3ac234a
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Device Details

"Rest" funnel chest correction system
TW: โ€œ่Šฎๆ€็‰นโ€ๆผๆ–—่ƒธ็Ÿฏๆญฃ็ณป็ตฑ
Risk Class 2

Registration Details

ae39fefe6d01392ada1a2243c3ac234a

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

Nov 23, 2022

Nov 23, 2027