Taiwan FDA registration e7758b533692596f140d527197173355

"Artron" MICROALBUMIN TEST(Non-Sterile)

TW: "雅創" 微白蛋白試劑 (未滅菌)

Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Mar 07, 2018 – Mar 07, 2023Expired

Registration details

Analysis ID: e7758b533692596f140d527197173355
License Form: Ministry of Health Medical Device Import No. 018874
Customs Code: DHA09401887402

Company information

Manufacturer: ARTRON LABORATORIES INC.
Manufacturer Country: Canada
Authorized Representative: GORED ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)".
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1645 Urine protein or albumin (non-quantitative) test system
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 07, 2018
Expiry Date: Mar 07, 2023

About this record

Access comprehensive regulatory information for "Artron" MICROALBUMIN 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 e7758b533692596f140d527197173355 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..

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