Taiwan FDA registration 125ce88f75caa2d5df6f99886aa7f3ea

"Torch Combination" Veterans Urine Antigen Rapid Diagnostic Test for Pneumonia (Unwiped Bacteria)

TW: 〝炬合〞退伍軍人肺炎尿液抗原快速診斷試劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·EIKEN CHEMICAL CO., LTD. NOGI PLANT.·Registered Jun 17, 2024 – Jun 17, 2029Active
Registration details
Analysis ID
125ce88f75caa2d5df6f99886aa7f3ea
Customs Code
DHA09402351102
Company information
Manufacturer Country
Japan
Product details
Intended Use
It is limited to the first-level identification scope of Haemophilus serum reagent (C.3300) in the classification and grading management method of medical devices.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3300 嗜血桿菌屬血清試劑
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Jun 17, 2024
Expiry Date
Jun 17, 2029
About this record

Access comprehensive regulatory information for "Torch Combination" Veterans Urine Antigen Rapid Diagnostic Test for Pneumonia (Unwiped Bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 125ce88f75caa2d5df6f99886aa7f3ea and manufactured by EIKEN CHEMICAL CO., LTD. NOGI PLANT.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

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