Lumi-Phos PRO - SFDA Registration ME0000014865SFDAA00061
Access comprehensive regulatory information for Lumi-Phos PRO 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 ME0000014865SFDAA00061 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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SFDA Official Data
1
ME0000014865SFDAA00061
Lumi-Phos PRO
SFDA Registration: ME0000014865SFDAA00061
Product Information
Buffered solution to be used with Immunoassay systems and reagents
Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000014865SFDAA00061
Authorization ID
MDMA-2-2023-0548
Status
Active
Expire Date
April 13, 2026
Manufacturer
Manufacturer Name
Beckman Coulter, Inc.Model Information
Model ID(s)
B96000
Product Accessories
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