Taiwan FDA registration 7e8012094bbcd15e5632ba44cf1437c4
"Leofisian" delivery medium (sterilized)
TW: “利奧菲森”輸送培養基(滅菌)
Taiwan·Risk Class 1·LIOFILCHEM S.R.L.·Registered Apr 14, 2022 – Apr 14, 2027ActiveRegistration details
- Analysis ID
- 7e8012094bbcd15e5632ba44cf1437c4
- Customs Code
- DHA09402278100
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 classification and grading management method of medical equipment "Conveying medium (C.2390)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2390 Transport culture medium
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Apr 14, 2022
- Expiry Date
- Apr 14, 2027
About this record
Access comprehensive regulatory information for "Leofisian" delivery 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 7e8012094bbcd15e5632ba44cf1437c4 and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices