Taiwan FDA registration dc19eb91f37cdab37c1cd284593c38d0

"All Souls" Influenza A and B Influenza Virus Antigen Fluorescence Test Kit (Unsterilized)

TW: "萬靈" A和B型流行性感冒病毒抗原螢光檢驗試驗套組 (未滅菌)

Taiwan·Risk Class 1·OXOID, LTD.·Registered Oct 27, 2010 – Oct 27, 2025Expired

Registration details

Analysis ID: dc19eb91f37cdab37c1cd284593c38d0
Customs Code: DHA04400942202

Company information

Manufacturer: OXOID, LTD.
Manufacturer Country: United Kingdom
Authorized Representative: WONDERFUL LIFE SCIENCE CO., LTD.

Product details

Intended Use: It is limited to the first-level identification scope of influenza virus serum reagent (C.3330) in the classification and grading management measures for medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3330 流感病毒血清試劑
Import Information: import

Dates and status

Registration Date: Oct 27, 2010
Expiry Date: Oct 27, 2025

About this record

Access comprehensive regulatory information for "All Souls" Influenza A and B Influenza Virus Antigen Fluorescence Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dc19eb91f37cdab37c1cd284593c38d0 and manufactured by OXOID, LTD.. The authorized representative in Taiwan is WONDERFUL LIFE SCIENCE CO., LTD..

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