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“OrthoDevelopment” Vusion OS System - Taiwan Registration ede2c86f227ef6beb05b4f7a0982b565

Access comprehensive regulatory information for “OrthoDevelopment” Vusion OS System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ede2c86f227ef6beb05b4f7a0982b565 and manufactured by ORTHO DEVELOPMENT CORPORATION. The authorized representative in Taiwan is Huixing Co., 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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ede2c86f227ef6beb05b4f7a0982b565
Registration Details
Taiwan FDA Registration: ede2c86f227ef6beb05b4f7a0982b565
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Device Details

“OrthoDevelopment” Vusion OS System
TW: “奧森迪威”腰椎間盤融合器
Risk Class 2
MD
Cancelled

Registration Details

ede2c86f227ef6beb05b4f7a0982b565

Ministry of Health Medical Device Import No. 028372

DHA05602837203

Company Information

United States

Product Details

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Apr 13, 2016

Apr 13, 2021

Aug 09, 2023

Cancellation Information

Logged out

許可證已逾有效期