Taiwan FDA registration a65d4d9c036d3b1086683af815b56a53
“Genoss” Osteon 3
TW: “吉諾斯”牙科骨粉
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Mar 14, 2022 – Mar 14, 2027ActiveRegistration details
- Analysis ID
- a65d4d9c036d3b1086683af815b56a53
- License Form
- Ministry of Health Medical Device Import No. 035295
- Customs Code
- DHA05603529502
Company information
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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
- Mar 14, 2022
- Expiry Date
- Mar 14, 2027
About this record
Access comprehensive regulatory information for “Genoss” Osteon 3 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a65d4d9c036d3b1086683af815b56a53 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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