Pure Global

DILUENT - ARCSA Registration 8357248138e9bb85ebab10b2505ffe03

Access comprehensive regulatory information for DILUENT in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 8357248138e9bb85ebab10b2505ffe03 and manufactured by ZYBIO INC. The device was registered on January 04, 2022.

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.

Free Database
Powered by Pure Global AI
ARCSA Official Data
I
8357248138e9bb85ebab10b2505ffe03
DILUENT
ARCSA ID: 8357248138e9bb85ebab10b2505ffe03
Local name: DILUYENTE
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Risk Class
I
Product Type
In Vitro Diagnostic
Brand Name
ZIBIO SERIES Z5
Commercial Name
17-740 ANALYZERS, LABORATORY, HEMATOLOGY
Registration Information
Analysis ID
8357248138e9bb85ebab10b2505ffe03
Registration Date
January 04, 2022
Expiration Date
January 04, 2027
Product Use

THE DILUENT IS A SOLUTION WITH SOME IONIC STRENGTH AND CONDUCTIVITY, WHICH CAN DILUTE THE BLOOD AND FORM THE FLUID, PROVIDING A STABLE ENVIRONMENT FOR BLOOD CELL COUNTING.

Manufacturer
City
CHONGQING
Country
CHINA
Address
FLOOR 1 TO FLOOR 4, BUILDING 30, NO.6 OF TAIKANG ROAD, BLOCK C OF JIANQIAO INDUSTRIAL PARK, DADUKOU DISTRICT, CHONGQING, CHINA 400082
Product Owner
Name
ZYBIO INC
Country
CHINA
Authorized Representative
Address
STREET: N88 NUMBER: 179 INTERSECTION: OE 2A
Phone
3441877