Taiwan FDA registration 87fae6cfc2fec23779d9839eef826ea9

"Nanotek" Influenza A and B Rapid Fluorescence Immunoassay Assay Kit (Unsterilized)

TW: “奈米鐵克” 流感病毒A型和B型快速螢光免疫分析檢測套組(未滅菌)

Taiwan·Risk Class 1·Nano-Ditech Corporation·Registered Mar 25, 2019 – Mar 25, 2024Expired

Registration details

Analysis ID: 87fae6cfc2fec23779d9839eef826ea9
Customs Code: DHA09402023400

Company information

Manufacturer: Nano-Ditech Corporation
Manufacturer Country: United States
Authorized Representative: GRAND MARQUIS CO., LTD.

Product details

Intended Use: It is limited to the first-level identification scope of influenza virus serum reagent (C.3330) in the "Microbial Sample Collection and Transportation Equipment (C.2900)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2900 Apparatus for collecting and delivering microbiological samples; C.3330 Influenza virus serum test
Import Information: import

Dates and status

Registration Date: Mar 25, 2019
Expiry Date: Mar 25, 2024

About this record

Access comprehensive regulatory information for "Nanotek" Influenza A and B Rapid Fluorescence Immunoassay Assay 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 87fae6cfc2fec23779d9839eef826ea9 and manufactured by Nano-Ditech Corporation. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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