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“Synthes” MatrixWAVE MMF System - Taiwan Registration 75ea13b22fc76ff9d5bffa3f0d71d65a

Access comprehensive regulatory information for “Synthes” MatrixWAVE MMF System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 75ea13b22fc76ff9d5bffa3f0d71d65a and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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75ea13b22fc76ff9d5bffa3f0d71d65a
Registration Details
Taiwan FDA Registration: 75ea13b22fc76ff9d5bffa3f0d71d65a
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Device Details

“Synthes” MatrixWAVE MMF System
TW: “信迪思”梅翠絲波浪顎骨固定系統
Risk Class 2
MD

Registration Details

75ea13b22fc76ff9d5bffa3f0d71d65a

Ministry of Health Medical Device Import No. 030971

DHA05603097104

Company Information

Switzerland

Product Details

This product is suitable for adults and adolescents (over 12 years old) who have developed permanent teeth for temporary treatment of upper and lower jaw fractures and osteotomy.

F Dental devices

F4760 bone plate

Imported from abroad

Dates and Status

Mar 07, 2018

Mar 07, 2023