Taiwan FDA registration fdca7f758e3ba429e98819659956dbe4
“Tutogen” CopiOs Pericardium Membrane
TW: “凸透晶”口美合牙科用膠原蛋白膜
Taiwan·Risk Class 2·MD·Tutogen Medical GmbH·Registered Nov 11, 2014 – Nov 11, 2024ExpiredRegistration details
- Analysis ID
- fdca7f758e3ba429e98819659956dbe4
- License Form
- Ministry of Health Medical Device Import No. 026782
- Customs Code
- DHA05602678202
Company information
- Manufacturer
- Tutogen Medical GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- HOWSHINE ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 11, 2014
- Expiry Date
- Nov 11, 2024
About this record
Access comprehensive regulatory information for “Tutogen” CopiOs Pericardium Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdca7f758e3ba429e98819659956dbe4 and manufactured by Tutogen Medical GmbH. The authorized representative in Taiwan is HOWSHINE ENTERPRISE CO., LTD..
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