Taiwan FDA registration f820d43ee3aa0a443046da50dec262d3
"Nefer" biosynthetic fiber membrane
TW: “奈菲兒”生物合成纖維膜
Taiwan·Risk Class 2·Oriental Innovation Development Co., Ltd. Biomedical Factory·Registered Jun 03, 2015 – Apr 07, 2019CancelledRegistration details
- Analysis ID
- f820d43ee3aa0a443046da50dec262d3
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Nefeier Biomedical Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jun 03, 2015
- Expiry Date
- Apr 07, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nefer" biosynthetic fiber membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f820d43ee3aa0a443046da50dec262d3 and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is Nefeier Biomedical Co., Ltd.
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