Taiwan FDA registration 8783582acf6261823b5232c4e00750e6

"All Souls" respiratory fusion virus antigen fluorescence test kit (unsterilized)

TW: "萬靈"呼吸道融合病毒抗原螢光檢驗試劑套組(未滅菌)

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

Registration details

Analysis ID: 8783582acf6261823b5232c4e00750e6
Customs Code: DHA04400942100

Company information

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

Product details

Intended Use: Limited to the classification and grading management of medical devices, the first level identification range of "respiratory fusion cell virus serum reagent (C.3480)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3480 呼吸道融合細胞病毒血清試劑
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" respiratory fusion 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 8783582acf6261823b5232c4e00750e6 and manufactured by OXOID LTD.. The authorized representative in Taiwan is WONDERFUL LIFE SCIENCE CO., LTD..

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