Taiwan FDA registration 4d5e05556812084448b2261b22914954
"Leofisian" fortified medium (sterilized)
TW: “利奧菲森”強化培養基(滅菌)
Taiwan·Risk Class 1·LIOFILCHEM S.R.L.·Registered Nov 17, 2021 – Nov 17, 2026ActiveRegistration details
- Analysis ID
- 4d5e05556812084448b2261b22914954
- Customs Code
- DHA09402270102
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 "Intensive Medium (C.2330)" of the Measures for the Classification and Grading Management of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2330 Enhanced culture medium
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 17, 2021
- Expiry Date
- Nov 17, 2026
About this record
Access comprehensive regulatory information for "Leofisian" fortified medium (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4d5e05556812084448b2261b22914954 and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..
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