Taiwan FDA registration c5f53cb9015e311dbbb1097acd575e72
“MegaGen” i-Gen Membrane
TW: “美佳”牙科鈦膜
Taiwan·Risk Class 2·MD·MEGAGEN IMPLANT CO., LTD.·Registered Oct 10, 2019 – Oct 10, 2024ExpiredRegistration details
- Analysis ID
- c5f53cb9015e311dbbb1097acd575e72
- License Form
- Ministry of Health Medical Device Import No. 032858
- Customs Code
- DHA05603285805
Company information
- Manufacturer
- MEGAGEN IMPLANT CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SUNRISER MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4760 bone plate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 10, 2019
- Expiry Date
- Oct 10, 2024
About this record
Access comprehensive regulatory information for “MegaGen” i-Gen Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5f53cb9015e311dbbb1097acd575e72 and manufactured by MEGAGEN IMPLANT CO., LTD.. The authorized representative in Taiwan is SUNRISER MEDICAL CO., LTD..
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