Saudi Arabia SFDA registration ME0000014865SFDAA00044
DXH ECO CELL LYSE
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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About this record
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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