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“Medacta” Mecta-C Stand Alone Anterior Cervical Interbody Fusion Device - Taiwan Registration 81da799c905c306fa6b8c6f8614ec3ce

Access comprehensive regulatory information for “Medacta” Mecta-C Stand Alone Anterior Cervical Interbody Fusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81da799c905c306fa6b8c6f8614ec3ce and manufactured by Medacta International SA. The authorized representative in Taiwan is LI MIN BIOTECH 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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81da799c905c306fa6b8c6f8614ec3ce
Registration Details
Taiwan FDA Registration: 81da799c905c306fa6b8c6f8614ec3ce
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Device Details

“Medacta” Mecta-C Stand Alone Anterior Cervical Interbody Fusion Device
TW: “美達特”美特西前側頸椎融合系統
Risk Class 2
MD

Registration Details

81da799c905c306fa6b8c6f8614ec3ce

Ministry of Health Medical Device Import No. 036115

DHA05603611505

Company Information

Switzerland

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Dec 01, 2022

Dec 01, 2027