Taiwan FDA registration 3af0419925f12ebb664edbcf2f2a728c
"Leofisian" selective medium (sterilized)
TW: “利奧菲森”選擇性培養基(滅菌)
Taiwan·Risk Class 1·LIOFILCHEM S.R.L.·Registered Dec 22, 2021 – Dec 22, 2026ActiveRegistration details
- Analysis ID
- 3af0419925f12ebb664edbcf2f2a728c
- Customs Code
- DHA09402271500
Company information
- Manufacturer
- LIOFILCHEM S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DiaTech Technology Co., Ltd.
Product details
- Intended Use
- Limited to the classification and grading management of medical devices "Selective culture medium (C.2360)" first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2360 選擇性培養基
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 22, 2021
- Expiry Date
- Dec 22, 2026
About this record
Access comprehensive regulatory information for "Leofisian" selective 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 3af0419925f12ebb664edbcf2f2a728c and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..
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