Taiwan FDA registration 1bc0bc0b1880a696238408687fb3aa82
"Lorne" Anti-E Monoclonal
TW: "羅倫"單株抗體抗E血清試劑
Taiwan·Risk Class 2·MD·Lorne Laboratories Ltd.·Registered Jan 15, 2019 – Jan 15, 2029ActiveRegistration details
- Analysis ID
- 1bc0bc0b1880a696238408687fb3aa82
- License Form
- Ministry of Health Medical Device Import No. 032116
- Customs Code
- DHA05603211600
Company information
- Manufacturer
- Lorne Laboratories Ltd.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- GLORY BIOSCIENCE CO., LTD.
Product details
- Intended Use
- Appraisal E blood type fraction.
- 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
- Jan 15, 2019
- Expiry Date
- Jan 15, 2029
About this record
Access comprehensive regulatory information for "Lorne" Anti-E Monoclonal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1bc0bc0b1880a696238408687fb3aa82 and manufactured by Lorne Laboratories Ltd.. The authorized representative in Taiwan is GLORY BIOSCIENCE CO., LTD..
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