Taiwan FDA registration 75ea13b22fc76ff9d5bffa3f0d71d65a
“Synthes” MatrixWAVE MMF System
TW: “信迪思”梅翠絲波浪顎骨固定系統
Taiwan·Risk Class 2·MD·SYNTHES GMBH·Registered Mar 07, 2018 – Mar 07, 2023ExpiredRegistration details
- Analysis ID
- 75ea13b22fc76ff9d5bffa3f0d71d65a
- License Form
- Ministry of Health Medical Device Import No. 030971
- Customs Code
- DHA05603097104
Company information
- Manufacturer
- SYNTHES GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4760 bone plate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 07, 2018
- Expiry Date
- Mar 07, 2023
About this record
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..
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