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“OrthoDevelopment” Vusion System (CS Plus) - Taiwan Registration 448ead39f87ef9feed860a06c775353a

Access comprehensive regulatory information for “OrthoDevelopment” Vusion System (CS Plus) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 448ead39f87ef9feed860a06c775353a 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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448ead39f87ef9feed860a06c775353a
Registration Details
Taiwan FDA Registration: 448ead39f87ef9feed860a06c775353a
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Device Details

“OrthoDevelopment” Vusion System (CS Plus)
TW: “奧森迪威”頸椎間盤融合器
Risk Class 2
MD
Cancelled

Registration Details

448ead39f87ef9feed860a06c775353a

Ministry of Health Medical Device Import No. 027491

DHA05602749106

Company Information

United States

Product Details

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Jul 07, 2015

Jul 07, 2020

Jun 16, 2022

Cancellation Information

Logged out

許可證已逾有效期未申請展延