Taiwan FDA registration f1955d8a86a40a654e2ffb6f92b40dba
Cytoplast RPM Reinforced PTFE Mesh
TW: 珊朵普拉斯亞琵原鈦增強聚四氟乙烯網膜
Taiwan·Risk Class 2·MD·Osteogenics Biomedical, Inc.·Registered Feb 14, 2022 – Feb 14, 2027ActiveRegistration details
- Analysis ID
- f1955d8a86a40a654e2ffb6f92b40dba
- License Form
- Ministry of Health Medical Device Import No. 035268
- Customs Code
- DHA05603526802
Company information
- Manufacturer
- Osteogenics Biomedical, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ALVIS MEDICAL EQUIPMENT CO., LTD
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F3930 Alveolar Restoration Materials
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 14, 2022
- Expiry Date
- Feb 14, 2027
About this record
Access comprehensive regulatory information for Cytoplast RPM Reinforced PTFE Mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f1955d8a86a40a654e2ffb6f92b40dba and manufactured by Osteogenics Biomedical, Inc.. The authorized representative in Taiwan is ALVIS MEDICAL EQUIPMENT CO., LTD.
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