Taiwan FDA registration 310e00cad0be4de9dc0c2343079971e9
Recording of Paz G Fetal Protein-N Test Reagent Standard
TW: 錄秘帕斯G甲型胎兒蛋白-N檢驗試劑標準液
Taiwan·Risk Class 2·Fujirebio Inc. Sagamihara Facility·Registered Jan 10, 2011 – Jan 10, 2026ExpiredRegistration details
- Analysis ID
- 310e00cad0be4de9dc0c2343079971e9
- Customs Code
- DHA00602193608
Company information
- Manufacturer
- Fujirebio Inc. Sagamihara Facility
- Manufacturer Country
- Japan
- Authorized Representative
- Grand Marquis IVD CO., LTD.
Product details
- Intended Use
- Calibration reagent specially used to record the detection reagent of Paz G Fetal Protein-N
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Jan 10, 2011
- Expiry Date
- Jan 10, 2026
About this record
Access comprehensive regulatory information for Recording of Paz G Fetal Protein-N Test Reagent Standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 310e00cad0be4de9dc0c2343079971e9 and manufactured by Fujirebio Inc. Sagamihara Facility. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..
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