Taiwan FDA registration c789853d8601a67c129c84025bbf0c70
LEIBO Synthetic Cell & Tissue Culture Media & Ingredients (Sterilized)
TW: 〝磊柏〞合成細胞和組織培養基及成份 (滅菌)
Taiwan·Risk Class 1·FUJIFILM Irvine Scientific, Inc.·Registered Feb 19, 2024 – Feb 19, 2029ActiveRegistration details
- Analysis ID
- c789853d8601a67c129c84025bbf0c70
- Customs Code
- DHA09402339000
Company information
- Manufacturer
- FUJIFILM Irvine Scientific, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- LabIVF Taiwan International Co., Ltd
Product details
- Intended Use
- It is limited to the first level of identification of synthetic cell and tissue culture media and ingredients (B.2220) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.2220 Synthetic cell and tissue culture media and components
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Feb 19, 2024
- Expiry Date
- Feb 19, 2029
About this record
Access comprehensive regulatory information for LEIBO Synthetic Cell & Tissue Culture Media & Ingredients (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c789853d8601a67c129c84025bbf0c70 and manufactured by FUJIFILM Irvine Scientific, Inc.. The authorized representative in Taiwan is LabIVF Taiwan International 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