Taiwan FDA registration c804101ab638863353fc1689397132d7

Inolaifu urine albumin and urine protein test reagents (unsterilized)

TW: 伊諾來富尿液白蛋白與尿蛋白檢查試劑(未滅菌)

Taiwan·Risk Class 1·PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.·Registered Aug 13, 2020 – Aug 13, 2025Expired

Registration details

Analysis ID: c804101ab638863353fc1689397132d7

Company information

Manufacturer: PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.

Product details

Intended Use: It is limited to the first level of identification of the "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)" and "Albumin Immunoassay System (C.5040)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
Product Type (Level 2): A.1645 Urine protein or albumin (non-quantitative) testing system; C.5040 Albumin immunoassay system
Import Information: Domestic

Dates and status

Registration Date: Aug 13, 2020
Expiry Date: Aug 13, 2025

About this record

Access comprehensive regulatory information for Inolaifu urine albumin and urine protein test reagents (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c804101ab638863353fc1689397132d7 and manufactured by PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.. The authorized representative in Taiwan is PROTECTLIFE INTERNATIONAL BIOMEDICAL INC..

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