Taiwan FDA registration bbd9ee2a3973b9504313d292c556179f

"ACRO" iGFBP-1 Rapid Test (Non-Sterile)

TW: "艾快露" 類胰島素生長因子結合蛋白-1快速檢驗試劑(未滅菌)

Taiwan·Risk Class 1·MD·ACRO BIOTECH. INC.·Registered May 24, 2018 – May 24, 2023Expired

Registration details

Analysis ID: bbd9ee2a3973b9504313d292c556179f
License Form: Ministry of Health Medical Device Import No. 019091
Customs Code: DHA09401909101

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 of identification range of the Measures for the Administration of Medical Devices "Uric pH (Non-quantitative) Test System (A.1550)".
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1550 Uric pH (non-quantitative) test system
Import Information: Imported from abroad

Dates and status

Registration Date: May 24, 2018
Expiry Date: May 24, 2023

About this record

Access comprehensive regulatory information for "ACRO" iGFBP-1 Rapid Test (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 bbd9ee2a3973b9504313d292c556179f and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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