Taiwan FDA registration 0f6df15e59914e04e0aded2fb0dbeb4f

“ACRO” fFN Rapid Test Cassette (Non-Sterile)

TW: “艾快露” 纖維黏連蛋白檢驗試劑 (未滅菌)

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

Registration details

Analysis ID: 0f6df15e59914e04e0aded2fb0dbeb4f
License Form: Ministry of Health Medical Device Import No. 019261
Customs Code: DHA09401926100

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 human growth hormone test system (A.1370) of the management measures for medical equipment.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1370 Human Growth Hormone Test System
Import Information: Imported from abroad

Dates and status

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

About this record

Access comprehensive regulatory information for “ACRO” fFN Rapid Test Cassette (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 0f6df15e59914e04e0aded2fb0dbeb4f and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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