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"Niostri" cell cryogenic equipment for in vitro diagnostics (unsterilized) - Taiwan Registration eb6c54f79e880bfc9419286492cccd17

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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eb6c54f79e880bfc9419286492cccd17
Registration Details
Taiwan FDA Registration: eb6c54f79e880bfc9419286492cccd17
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Device Details

"Niostri" cell cryogenic equipment for in vitro diagnostics (unsterilized)
TW: "ๅฆฎๅ‚ฒ็ตฒ็ฟ " ้ซ”ๅค–่จบๆ–ท็”จ็ดฐ่ƒžๅ†ทๅ‡่จญๅ‚™ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

eb6c54f79e880bfc9419286492cccd17

Company Information

Taiwan, Province of China

Product Details

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.

B Hematology, pathology, and genetics

B.9225 Cell freezing equipment and reagents for in vitro diagnostics

Domestic

Dates and Status

Mar 25, 2015

Mar 25, 2025