Taiwan FDA registration b4c151159b0b5b40fdc3bc82b1d358aa

"Echoroll" Respiratory Fusion Virus Test Reagent (Non-sterile)

TW: "愛可羅" 呼吸道融合病毒檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·ACRO BIOTECH. INC.·Registered Oct 27, 2023 – Oct 27, 2028Active

Registration details

Analysis ID: b4c151159b0b5b40fdc3bc82b1d358aa
Customs Code: DHA09402329101

Company information

Manufacturer: ACRO BIOTECH. INC.
Manufacturer Country: United States
Authorized Representative: APPLIED BIOTECH ENTERPRISE 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: Input;; QMS/QSD

Dates and status

Registration Date: Oct 27, 2023
Expiry Date: Oct 27, 2028

About this record

Access comprehensive regulatory information for "Echoroll" Respiratory Fusion Virus Test Reagent (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4c151159b0b5b40fdc3bc82b1d358aa and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..

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