Taiwan FDA registration 355ba89a3a1fe6b4e120820ffa55cb46

"Oxel Doctor" parainfluenza virus antigen fluorescence test set (unsterilized)

TW: "歐克索醫"副流行性感冒病毒抗原螢光檢驗試劑組(未滅菌)

Taiwan·Risk Class 1·OXOID LTD·Registered Apr 12, 2011 – Apr 12, 2026Expired

Registration details

Analysis ID: 355ba89a3a1fe6b4e120820ffa55cb46
Customs Code: DHA04401018103

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 the "Parainfluenza Virus Serum Reagent (C.3400)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3400 Parainfluenza Virus Seroblast
Import Information: import

Dates and status

Registration Date: Apr 12, 2011
Expiry Date: Apr 12, 2026

About this record

Access comprehensive regulatory information for "Oxel Doctor" parainfluenza virus antigen fluorescence test set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 355ba89a3a1fe6b4e120820ffa55cb46 and manufactured by OXOID LTD. The authorized representative in Taiwan is WONDERFUL LIFE SCIENCE CO., LTD..

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