Taiwan FDA registration caaa4a1cedbcc2b78435e89077a43011
“Lorne” Anti-Fya Monoclonal
TW: “羅倫” 單株抗體抗Fya血清試劑
Taiwan·Risk Class 2·MD·Lorne Laboratories Limited·Registered Jun 30, 2017 – Jun 30, 2027ActiveRegistration details
- Analysis ID
- caaa4a1cedbcc2b78435e89077a43011
- License Form
- Ministry of Health Medical Device Import No. 029587
- Customs Code
- DHA05602958703
Company information
- Manufacturer
- Lorne Laboratories Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- GLORY BIOSCIENCE CO., LTD.
Product details
- Intended Use
- This product uses indirect antiglobulin method to detect Fya antigen in human red blood cells.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B4020 Analyze specific reagents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 30, 2017
- Expiry Date
- Jun 30, 2027
About this record
Access comprehensive regulatory information for “Lorne” Anti-Fya Monoclonal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number caaa4a1cedbcc2b78435e89077a43011 and manufactured by Lorne Laboratories Limited. The authorized representative in Taiwan is GLORY BIOSCIENCE CO., LTD..
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