Taiwan FDA registration e3440070da5b89c395a975f051288852
“Lorne” Anti-Jka Polyclonal
TW: “羅倫” 多株抗體抗Jka血清試劑
Taiwan·Risk Class 2·MD·Lorne Laboratories Limited·Registered Jul 18, 2017 – Jul 18, 2022ExpiredRegistration details
- Analysis ID
- e3440070da5b89c395a975f051288852
- License Form
- Ministry of Health Medical Device Import No. 029594
- Customs Code
- DHA05602959400
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 Jka 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
- Jul 18, 2017
- Expiry Date
- Jul 18, 2022
About this record
Access comprehensive regulatory information for “Lorne” Anti-Jka Polyclonal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3440070da5b89c395a975f051288852 and manufactured by Lorne Laboratories Limited. The authorized representative in Taiwan is GLORY BIOSCIENCE CO., LTD..
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