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DXH ECO CELL LYSE - SFDA Registration ME0000014865SFDAA00044

Access comprehensive regulatory information for DXH ECO CELL LYSE in the Saudi Arabia medical device market through Pure Global AI's free database. This 1 device is registered with Saudi Arabia SFDA under registration number ME0000014865SFDAA00044 and manufactured by Beckman Coulter, Inc..

This page provides complete registration details including product category (IVD), 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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1
ME0000014865SFDAA00044
DXH ECO CELL LYSE
SFDA Registration: ME0000014865SFDAA00044
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Product Information

Erythrocyte lytic agent for quantitative determination of hemoglobin enumeration of NRBC and counting and sizing leukocytes

Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000014865SFDAA00044
Authorization ID
MDMA-2-2025-0330
Status
Active
Expire Date
January 27, 2028
Manufacturer
Manufacturer Name
Beckman Coulter, Inc.
Model Information
Model ID(s)
C67251 C67252
Product Accessories

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