Taiwan FDA registration ed05bbce2ad0863c55fd30bae8bc9bfb
“Genoss” Collagen Membrane
TW: “吉諾斯”膠原膜
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Apr 04, 2020 – Apr 04, 2025ExpiredRegistration details
- Analysis ID
- ed05bbce2ad0863c55fd30bae8bc9bfb
- License Form
- Ministry of Health Medical Device Import No. 033432
- Customs Code
- DHA05603343202
Company information
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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)
- F3930 Alveolar Restoration Materials
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 04, 2020
- Expiry Date
- Apr 04, 2025
About this record
Access comprehensive regulatory information for “Genoss” Collagen Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed05bbce2ad0863c55fd30bae8bc9bfb and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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