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Yumizen H2500 - SFDA Registration ME0000002480SFDAA00064

Access comprehensive regulatory information for Yumizen H2500 in the Saudi Arabia medical device market through Pure Global AI's free database. This General IVD(Others) device is registered with Saudi Arabia SFDA under registration number ME0000002480SFDAA00064 and manufactured by HORIBA ABX SAS.

This page provides complete registration details including product category (Chemicals), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.

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General IVD(Others)
ME0000002480SFDAA00064
Yumizen H2500
SFDA Registration: ME0000002480SFDAA00064
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Product Information

Hematology analyzer for use in clinical laboratories.

Product Use

The Yumizen H2500 is a quantitative multi-parameter, automated hematology analyzer for in vitro diagnostic use in screening patient populations found in clinical laboratories

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000002480SFDAA00064
Authorization ID
MDMA-1-2019-2385
Status
Active
Expire Date
May 27, 2025
Manufacturer
Manufacturer Name
HORIBA ABX SAS
Model Information
Model ID(s)
Yumizen H2500
Product Accessories

[{'tradeName': 'Yumizen SPS', 'description': ' preparation and staining of a sample blood smear', 'gmdn': 'N/A'}]