5fa1cce74bce326928a53d2126257276
Fibrinogen reagent kit (clotting)
GUANGZHOU WONDFO BIOTECH CO. LTDA·III·Ecuador ARCSA·Registered April 30, 2023
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
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
Product use
DETERMINATION OF FIBRINOGEN FIB REAGENTS
About this record
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.