Taiwan FDA registration f1fc58d3a50dd9801c39c1e71565b8c8
"Leofisen" quality control strain (unsterilized)
TW: “利奧菲森” 品管菌株(未滅菌)
Taiwan·Risk Class 1·LIOFILCHEM S.R.L.·Registered Jul 04, 2023 – Jul 04, 2028ActiveRegistration details
- Analysis ID
- f1fc58d3a50dd9801c39c1e71565b8c8
- Customs Code
- DHA09402317203
Company information
- Manufacturer
- LIOFILCHEM S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DiaTech Technology Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of the quality management equipment group (C.2480) of the culture medium for classification and grading management of medical equipment.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2480 培養基的品質管制器材組
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jul 04, 2023
- Expiry Date
- Jul 04, 2028
About this record
Access comprehensive regulatory information for "Leofisen" quality control strain (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f1fc58d3a50dd9801c39c1e71565b8c8 and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..
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