Taiwan FDA registration 4293a9f622276b3b22156be787046815
“Medentika” M-Implant Endosseous Implant prosthetic parts
TW: “麥登狄卡”艾姆植體骨內植體補綴零件
Taiwan·Risk Class 2·MD·MEDENTiKA GmbH·Registered Jul 28, 2014 – Jul 28, 2024ExpiredRegistration details
- Analysis ID
- 4293a9f622276b3b22156be787046815
- License Form
- Ministry of Health Medical Device Import No. 026355
- Customs Code
- DHA05602635506
Company information
- Manufacturer
- MEDENTiKA GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- Straumann Group (Taiwan) 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)
- F3630 Dental bridges for bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 28, 2014
- Expiry Date
- Jul 28, 2024
About this record
Access comprehensive regulatory information for “Medentika” M-Implant Endosseous Implant prosthetic parts in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4293a9f622276b3b22156be787046815 and manufactured by MEDENTiKA GmbH. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..
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