Taiwan FDA registration c7aabba4fa70aa365837b93dce29330c

"Ai Kuailu" Respiratory Fusion Cell Virus/A+B Influenza Rapid Test Kit (Unsterilized)

TW: "艾快露"呼吸道融合細胞病毒/A+B型流行性感冒快速檢驗套組 (未滅菌)

Taiwan·Risk Class 1·ACRO BIOTECH. INC.·Registered Jul 04, 2018 – Jul 04, 2023Expired

Registration details

Analysis ID: c7aabba4fa70aa365837b93dce29330c
Customs Code: DHA09401926202

Company information

Manufacturer: ACRO BIOTECH. INC.
Manufacturer Country: United States
Authorized Representative: Grand Marquis IVD CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)" and "Respiratory Fusion Cell Virus Serum Reagent (C.3480)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3330 流感病毒血清試劑;; C.3480 呼吸道融合細胞病毒血清試劑
Import Information: import

Dates and status

Registration Date: Jul 04, 2018
Expiry Date: Jul 04, 2023

About this record

Access comprehensive regulatory information for "Ai Kuailu" Respiratory Fusion Cell Virus/A+B Influenza Rapid 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 c7aabba4fa70aa365837b93dce29330c and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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