Taiwan FDA registration 9633402e66d675a2aca586837d4b6fb2
"Loren" anti-human IgG serum reagent
TW: “羅倫”抗人類IgG血清試劑
Taiwan·Risk Class 2·Lorne Laboratories Limited·Registered Jul 02, 2019 – Jul 02, 2029ActiveRegistration details
- Analysis ID
- 9633402e66d675a2aca586837d4b6fb2
- Customs Code
- DHA05603245700
Company information
- Manufacturer
- Lorne Laboratories Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- GLORY BIOSCIENCE CO., LTD.
Product details
- Intended Use
- Red blood cell IgG is detected using a direct or indirect antiglobulin test.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4020 Analysis of specific tests
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 02, 2019
- Expiry Date
- Jul 02, 2029
About this record
Access comprehensive regulatory information for "Loren" anti-human IgG serum reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9633402e66d675a2aca586837d4b6fb2 and manufactured by Lorne Laboratories Limited. The authorized representative in Taiwan is GLORY BIOSCIENCE CO., LTD..
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