Fibrinogen reagent kit (clotting) - ARCSA Registration 5fa1cce74bce326928a53d2126257276
Access comprehensive regulatory information for Fibrinogen reagent kit (clotting) in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 5fa1cce74bce326928a53d2126257276 and manufactured by GUANGZHOU WONDFO BIOTECH CO. LTDA. The device was registered on April 30, 2023.
This page provides complete registration details including product type (In Vitro Diagnostic), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
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ARCSA Official Data
III
5fa1cce74bce326928a53d2126257276
Fibrinogen reagent kit (clotting)
ARCSA ID: 5fa1cce74bce326928a53d2126257276
Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Brand Name
WONDFO
Commercial Name
17-048 IVD Reagents/Testing Kits, Hematology, Coagulation
Registration Information
Analysis ID
5fa1cce74bce326928a53d2126257276
Registration Date
April 30, 2023
Expiration Date
April 30, 2028
Product Use
DETERMINATION OF FIBRINOGEN FIB REAGENTS
Manufacturer
City
GUANGZHOU
Country
CHINA
Address
# 8 LIZHISHAN ROAD, SCIENCE CITY LUOGANG DISTRICT 510663 GUANGZHOU
Product Owner
Name
GUANGZHOU WONDFO BIOTECH CO. LTDA
Country
CHINA
Authorized Representative
Address
NEIGHBORHOOD: COOP DE VIVIENDA SERVIDORES Y MANZANA:21 CALLE:AVENIDA JUANTANCA MARENGO, SOLAR 5 INTERSECTION: SN
Phone
42233672