Taiwan FDA registration 3349393d3250fe698806d29d04c9589f

K-Arthur Fibrinogen Analysis Reagent

TW: 克-亞瑟纖維蛋白原分析試劑

Taiwan·Risk Class 2·KAMIYA BIOMEDICAL COMPANY·Registered Aug 21, 2006 – Aug 21, 2021Cancelled

Registration details

Analysis ID: 3349393d3250fe698806d29d04c9589f
Customs Code: DHA00601728902

Company information

Manufacturer: KAMIYA BIOMEDICAL COMPANY
Manufacturer Country: United States
Authorized Representative: REDOX BIOMEDICINE CO., LTD.

Product details

Intended Use: It is used to quantitatively determine the value of fibrinogen in plasma.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.7340 Fibrinogen Confirmation System
Import Information: import

Dates and status

Registration Date: Aug 21, 2006
Expiry Date: Aug 21, 2021
Cancellation Date: Oct 06, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for K-Arthur Fibrinogen Analysis Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3349393d3250fe698806d29d04c9589f and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is REDOX BIOMEDICINE CO., LTD..

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