Taiwan FDA registration eb6c54f79e880bfc9419286492cccd17
"Niostri" cell cryogenic equipment for in vitro diagnostics (unsterilized)
TW: "妮傲絲翠" 體外診斷用細胞冷凍設備 (未滅菌)
Taiwan·Risk Class 1·Niostria Co., Ltd. Biomedical Factory·Registered Mar 25, 2015 – Mar 25, 2025ExpiredRegistration details
- Analysis ID
- eb6c54f79e880bfc9419286492cccd17
Company information
- Manufacturer
- Niostria Co., Ltd. Biomedical Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- NEOASIA LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical devices, "Cell cryonics equipment and reactants for in vitro diagnosis (B.9225)" Grade 1 identification range.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9225 Cell freezing equipment and reagents for in vitro diagnostics
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 25, 2015
- Expiry Date
- Mar 25, 2025
About this record
Access comprehensive regulatory information for "Niostri" cell cryogenic equipment for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eb6c54f79e880bfc9419286492cccd17 and manufactured by Niostria Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is NEOASIA LTD..
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